Archive
Genetic Center
Filatov's Child Clinical Hospital © 2001-2004
Vladimir Solonichenko MD, Clinical Geneticist,©
E-mail:
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Archive
- January 31, 2001
- February 2, 2001
- February 8, 2001
- February 12, 2001
- February 20, 2001
- February 27, 2001
- March 1, 2001
- March 7, 2001
- March 15, 2001
- March 28, 2001
- April 5, 2001
- April 13, 2001
- April 17, 2001
- April 25, 2001
- April 28, 2001
- May 12, 2001
- May 25, 2001
- May 31, 2001
- June 2, 2001
- June 7, 2001
- June 13, 2001
- June 18, 2001
- June 25, 2001
- July 3, 2001
- July 7, 2001
- July 22, 2001
- July 26, 2001
- July 31, 2001
- August 2, 2001
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- August 7, 2001
- August 10, 2001
- August 15, 2001
- August 17, 2001
- August 22, 2001
- August 25, 2001
- August 29, 2001
- August 31, 2001
- September 5, 2001
- September 8, 2001
- September 11, 2001
- September 14, 2001
- September 17, 2001
- September 20, 2001
- September 22, 2001
- September 25, 2001
- September 28, 2001
- September 30, 2001
- October 3, 2001
- October 5, 2001
- October 9, 2001
- October 11, 2001
- October 13, 2001
- October 17, 2001
- October 20, 2001
- October 21, 2001
- October 22, 2001
- October 24, 2001
- October 26, 2001
- October 28, 2001
- October 31, 2001
- November 2, 2001
- November 6, 2001
- November 10, 2001
- November 14, 2001
- November 17, 2001
- November 19, 2001
- November 21, 2001
- November 23, 2001
- November 25, 2001
- November 27, 2001
- November 29, 2001
- December 3, 2001
- December 6, 2001
- December 9, 2001
- December 12, 2001
- December 14, 2001
- December 18, 2001
- December 20, 2001
- December 23, 2001
- December 28, 2001
- January 10, 2002
- January 12, 2002
- January 16, 2002
- January 21, 2002
- January 24, 2002
- January 27, 2002
- January 31, 2002
- February 3, 2002
- February 7, 2002
- February 11, 2002
- February 14, 2002
- February 17, 2002
- February 21, 2002
- February 25, 2002
- February 28, 2002
- March 6, 2002
- March 11, 2002
- March 14, 2002
- March 17, 2002
- March 20, 2002
- March 23, 2002
- March 27, 2002
- March 30, 2002
- April 3, 2002
- April 6, 2002
- April 13, 2002
- April 17, 2002
- April 21, 2002
- April 25, 2002
- April 29, 2002
- May 8, 2002
- May 12, 2002
- May 15, 2002
- May 18, 2002
- May 22, 2002
- May 25, 2002
- May 28, 2002
- May 31, 2002
- June 3, 2002
- June 6, 2002
- June 8, 2002
- June 12, 2002
- June 14, 2002
- June 17, 2002
- June 19, 2002
- June 22, 2002
- June 25, 2002
- June 27, 2002
- June 30, 2002
- July 3, 2002
- July 6, 2002
- July 10, 2002
- July 13, 2002
- July 17, 2002
- July 20, 2002
- July 28, 2002
- July 31, 2002
- August 5, 2002
- August 10, 2002
- August 15, 2002
- August 18, 2002
- August 20, 2002
- August 22, 2002
- August 24, 2002
- August 26, 2002
- August 28, 2002
- August 30, 2002
- September 2, 2002
- September 4, 2002
- September 6, 2002
- September 9, 2002
- September 11, 2002
- September 13, 2002
- September 16, 2002
- September 18, 2002
- September 20, 2002
- September 23, 2002
- September 25, 2002
- September 27, 2002
- September 30, 2002
- October 2, 2002
- October 4, 2002
- October 7, 2002
- October 9, 2002
- October 11, 2002
- October 14, 2002
- October 16, 2002
- October 18, 2002
- October 21, 2002
- October 23, 2002
- October 25, 2002
- October 28, 2002
- October 30, 2002
- November 1, 2002
- November 4, 2002
- November 6, 2002
- November 8, 2002
- November 11, 2002
- November 13, 2002
- November 15, 2002
- November 18, 2002
- November 20, 2002
- November 22, 2002
- November 25, 2002
- November 27, 2002
- November 29, 2002
- December 2, 2002
- December 4, 2002
- December 6, 2002
- December 9, 2002
- December 11, 2002
- December 13, 2002
- December 15, 2002
- December 18, 2002
- December 20, 2002
- December 21, 2002
- December 23, 2002
- December 25, 2002
- December 27, 2002
- December 29, 2002
- December 31, 2002
- January 5, 2003
- January 10, 2003
- January 13, 2003
- January 15, 2003
- January 17, 2003
- January 20, 2003
- January 22, 2003
- January 24, 2003
- January 27, 2003
- January 29, 2003
- January 31, 2003
- February 3, 2003
- February 5, 2003
- February 7, 2003
- February 10, 2003
- February 12, 2003
- February 14, 2003
- February 17, 2003
- February 19, 2003
- February 21, 2003
- February 24, 2003
- February 27, 2003
- February 28, 2003
- March 3, 2003
- March 5, 2003
- March 7, 2003
- March 10, 2003
- March 12, 2003
- March 14, 2003
- March 17, 2003
- March 19, 2003
- March 21, 2003
- March 24, 2003
- March 26, 2003
- March 28, 2003
- March 31, 2003
- April 2, 2003
- April 4, 2003
- April 7, 2003
- April 9, 2003
- April 11, 2003
- April 13, 2003
- April 15, 2003
- April 17, 2003
- April 19, 2003
- April 21, 2003
- April 23, 2003
- April 25, 2003
- April 27, 2003
- April 29, 2003
- May 1, 2003
- May 3, 2003
- May 5, 2003
- May 7, 2003
- May 9, 2003
- May 11, 2003
- May 13, 2003
- May 15, 2003
- May 17, 2003
- May 19, 2003
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- May 25, 2003
- May 27, 2003
- May 29, 2003
- May 31, 2003
- June 2, 2003
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- June 6, 2003
- June 8, 2003
- June 10, 2003
- June 12, 2003
- June 16, 2003
- June 18, 2003
- June 20, 2003
- June 22, 2003
- June 24, 2003
- June 26, 2003
- June 28, 2003
- June 30, 2003
- July 2, 2003
- July 5, 2003
- July 7, 2003
- July 9, 2003
- July 11, 2003
- July 14, 2003
- July 16, 2003
- July 18, 2003
- July 21, 2003
- July 23, 2003
- July 25, 2003
- July 28, 2003
- July 30, 2003
- August 1, 2003
- August 4, 2003
- August 6, 2003
- August 8, 2003
- August 11, 2003
- August 13, 2003
- August 15, 2003
- August 18, 2003
- August 20, 2003
- August 22, 2003
- August 25, 2003
- August 27, 2003
- August 29, 2003
- September 1, 2003
- September 3, 2003
- September 5, 2003
- September 8, 2003
- September 10, 2003
- September 12, 2003
- September 15, 2003
- September 17, 2003
- September 19, 2003
- September 22, 2003
- September 24, 2003
- September 26, 2003
- September 29, 2003
- October 1, 2003
- October 3, 2003
- October 6, 2003
- October 8, 2003
- October 10, 2003
- October 13, 2003
- October 15, 2003
- October 17, 2003
- October 20, 2003
- October 22, 2003
- October 24, 2003
- October 27, 2003
- October 29, 2003
- October 31, 2003
- November 3, 2003
- November 5, 2003
- November 7, 2003
- November 10, 2003
- November 12, 2003
- November 14, 2003
- November 17, 2003
- November 19, 2003
- November 21, 2003
- November 24, 2003
- November 26, 2003
- November 28, 2003
- December 1, 2003
- December 3, 2003
- December 5, 2003
- December 8, 2003
- December 10, 2003
- December 12, 2003
- December 15, 2003
- December 22, 2003
- December 29, 2003
- January 5, 2004
- January 12, 2004
- January 19, 2004
- January 26, 2004
- February 2, 2004
- February 9, 2004
- February 16, 2004
- February 23, 2004
- March 1, 2004
- March 8, 2004
- March 15, 2004
- March 22, 2004
- March 29, 2004
- April 5, 2004
- April 12, 2004
- April 19, 2004
- April 26, 2004
- May 5, 2004
- May 11, 2004
- May 17, 2004
- May 24, 2004
- May 31, 2004
- June 7, 2004
- June 14, 2004
- June 21, 2004
- June 28, 2004
- July 5, 2004
- July 12, 2004
- July 19, 2004
- July 26, 2004
- August 2, 2004
- August 9, 2004
- August 16, 2004
- August 23, 2004
- August 30, 2004
- September 6, 2004
- September 13, 2004
- September 20, 2004
- September 26, 2004
- September 30, 2004
- October 2, 2004
- October 5, 2004
- October 9, 2004
- October 14, 2004
- October 20, 2004
- October 23, 2004
- October 28, 2004
- November 1, 2004
- November 4, 2004
- November 8, 2004
- November 12, 2004
- November 14, 2004
- November 18, 2004
- November 18, 2004
- November 22, 2004
- November 25, 2004
- November 29, 2004
- December 3, 2004
- December 7, 2004
- December 11, 2004
- December 17, 2004
- December 20, 2004
- December 24, 2004
- December 28, 2004
- December 31, 2004
- January 4, 2005
- January 7, 2005
- January 10, 2005
- January 14, 2005
- January 18, 2005
- January 22, 2005
- January 25, 2005
- January 28, 2005
- January 31, 2005
- February 4, 2005
- February 8, 2005
- February 11, 2005
- February 15, 2005
- February 18, 2005
- February 22, 2005
- February 25, 2005
- March 1, 2005
- March 4, 2005
- March 8, 2005
- March 11, 2005
- March 15, 2005
- March 18, 2005
- March 22, 2005
- March 29, 2005
- April 29, 2005
- May 31, 2005
- June 30, 2005
- July 29, 2005
- August 30, 2005
- September 28, 2005
- October 28, 2005
- November 29, 2005
- December 30, 2005
- January 30, 2006
- February 25, 2006
- March 26, 2006
- April 23, 2006
- May 26, 2006
- June 26, 2006
- July 26, 2006
- August 26, 2006
- September 24, 2006
- October 30, 2006
- November 26, 2006
- December 24, 2006
- January 28, 2007
- February 25, 2007
- March 25, 2007
- April 30, 2007
- May 28, 2007
- June 22, 2007
- July 23, 2007
- August 26, 2007
- September 23, 2007
- October 31, 2007
- November 26, 2007
- December 17, 2007
- January 28, 2008
- February 25, 2008
- March 27, 2008
- April 22, 2008
- May 25, 2008
- June 30, 2008
- July 25, 2008
- August 29, 2008
- September 27, 2008
- October 25, 2008
- November 22, 2008
- December 29, 2008
- January 25, 2009
- February 23, 2009
- March 30, 2009
- April 20, 2009
January 31, 2001
February 2, 2001
February 8, 2001
February 12, 2001
February 20, 2001
February 27, 2001
March 1, 2001
March 7, 2001
March 15, 2001
March 28, 2001
April 5, 2001
- A COL1A1 Sp1 binding site polymorphism predisposes to osteoporotic fracture by affecting bone density and quality
- A Complete Map of the Human Ribosomal Protein Genes.Assignment of 80 Genes to the Cytogenetic Map and Implications for Human Disorders
- A Genomewide Screen in Multiplex Rheumatoid Arthritis Families Suggests Genetic Overlap with Other Autoimmune Diseases
- ACTH-receptor-expression, regulation, and role in adrenocortical tumor formation
- Adrenoleukodystrophy.Incidence, new mutation rate, and results of extended family screening
- Amyotrophic Lateral Sclerosis Overview-GeneClinics
- An Extensive Analysis of Y-Chromosomal Microsatellite Haplotypes in Globally Dispersed Human Populations
- Angelman syndrome phenotype associated with mutations in MECP2, a gene encoding a methyl CpG binding protein
- Bleeding tendency in Wolfram syndrome,a newly identified feature with phenotype genotype correlation
- Characterization of Clustered MHC-Linked Olfactory Receptor Genes in Human and Mouse
- Cloning, characterization and chromosome mapping of the human SOX6 gene
- Common variants in the regulatory region of the insulin gene are associated with fasting plasma insulin levels in juvenile obesity
- Cystic Fibrosis - GeneClinics
- Cystinosis - GeneClinics
- Encyclopedia of Life Sciences
- Fabry disease-twenty novel alpha-galactosidase A mutations causing the classical phenotype
- Familial aggregation of QT-interval variability in a general population-results from the NHLBI Family Heart Study
- Fetal cells in transcervical samples at an early stage of gestation
- Final height in isolated growth hormone deficiency type 1A,effects of a 5-year treatment with insulin-like growth factor-I
- Folate, Homocysteine and Neural Tube Defects. An Overview
- Gene therapy-development of immunostimulatory treatments for cancer.
- Genetic and physiological analysis of the role of uncoupling proteins in human energy homeostasis
- Genetic Diversity of the Human Serotonin Receptor 1B (HTR1B) Gene
- Genetic susceptibility in infectious diseases.
- Helicobacter pylori genetic diversity and risk of human disease
- Holoprosencephaly due to mutations in ZIC2-alanine tract expansion mutations may be caused by parental somatic recombination
- Human mitochondrial genetics.
- Identification of two de novo partial trisomies by comparative genomic hybridization.
- Legal and Policy Issues in Genetics and Insurance
- Linkage of prostate cancer susceptibility loci to chromosome 1
- Males with anorexia nervosa.A controlled study of eating disorders in first-degree relatives
- Meta-analysis for linkage to asthma and atopy in the chromosome 5q31–33 candidate region
- Molecular polymorphism of O alleles in five populations of different ethnic origins
- Multicultural education and genetic counseling.
- Mutational screening of the cationic trypsinogen gene in a large cohort of subjects with idiopathic chronic pancreatitis.
- Obesity genes - Editorials, BMJ 2001
- Olfactory ReceptorGene Clusters, Genomic-Inversion Polymorphisms, and Common Chromosome Rearrangements
- Perfusion magnetic resonance abnormalities in patients with sickle cell disease
- Phenotypic effects of balanced X-autosome translocations in females-a retrospective survey of 104 cases reported from UK laboratories
- Primary progressive aphasia
- Protein kinase A in Carney Complex, a new example of cAMP pathway alteration in endocrine tumors
- Recombinant Down syndrome-a case report and literature review.
- Searching for genes underlying normal variation in human adiposity
- Sex determination-lessons from families and embryos
- Shakespeare as a geneticist.
- Simpson Golabi Behmel Syndrome.Progress toward Understanding the Molecular Basis for Overgrowth, Malformation, and Cancer Predisposition
- The pleiotropic functions of peroxisome proliferator-activated receptor
- The role of genomic imprinting in human developmental disorders. lessons from Prader-Willi syndrome.
- Tools for molecular genetic epidemiology-a comparison of MADGE methodology with other systems.
- Tsp509I polymorphism in exon 2 of the glucocorticoid receptor gene in relation to obesity and cortisol secretion-cohort study
- Von Hippel–Lindau Disease Masquerading as Autosomal Dominant Polycystic Kidney Disease
- Whole-Genome Screening in Ankylosing Spondylitis.Evidence of Non-MHC Genetic-Susceptibility Loci
April 13, 2001
April 17, 2001
- A mitotically stable marker chromosome negative for whole chromosome libraries, centromere probes and chromosome specific telomere regions-a novel class of supernumerary marker chromosome
- Alternative Ribonucleic Acid Processing in Endocrine Systems.
- Angiotensin receptors-distribution, signalling and function.
- Biochemical screening for chromosomal disorders and neural tube defects (NTD)...
- Birth weight and parental PGM1 alleles
- Characterization and geographic distribution of the low density lipoprotein receptor (LDLR) gene mutations in northwestern Greece
- Effect of pharmacogenetics on medicine
- Familial Excess Longevity in Utah Genealogies
- Folate, Homocysteine and Neural Tube Defects.An Overview
- Genetic and Phenotypic Markers Among Centenarians
- Genetic population history relationships of the population of Bogota, Colombia, by using the D1S80, VWA, and TH01 molecular markers
- Germline and somatic mutation analyses in the DNA mismatch repair gene MLH3.Evidence for somatic mutation in colorectal cancers
- Human DNA repair genes
- Insulin Resistance.Cellular and Clinical Concepts
- Interpretation, Design, and Analysis of Gene Array Expression Experiments
- LDL receptor cDNA sequence analysis in familial hypercholesterolemia patients...
- Leukocyte arylsulfatase A activity in patients with alcohol-related cirrhosis
- Longevity and the 2 Allele of Apolipoprotein E Longevity and the 2 Allele of Apolipoprotein E
- Mapping of genes and transcribed sequences in a gene rich 400-kb region on human chromosome 11p15.1p14
- Mice and men waltz together towards an understanding of hereditary deafness.
- Mucolipidosis type IV.Novel MCOLN1 mutations in Jewish and non-Jewish patients and the frequency of the disease in the Ashkenazi Jewish population
- Pendred syndrome, DFNB4, and PDS-SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations
- Prenatal detection of free sialic acid storage disease-genetic and biochemical studies in nine families
- Searching for Human Longevity Genes
- Spectrum of germline RB1 gene mutations in Spanish retinoblastoma patients.Phenotypic and molecular epidemiological implications
- The ethics of benefit sharing.
- The human Y chromosome derives largely from a single autosomal region added to the sex chromosomes 80-130 million years ago
- The New Human Tissue Kallikrein Gene Family.Structure, Function, and Association to Disease.
- Towards a vaccine for Alzheimer disease.
- Treating a mouse model for Sly disease with a novel form of gene therapy
- Usefulness of genetic susceptibility and biomarkers for evaluation of environmental health risk
- Variable expressivity and mutation databases.The androgen receptor gene mutations database
- WFS1-wolframin mutations, Wolfram syndrome, and associated diseases
- X-Linked Agammaglobulinemia - GeneClinic
- Y Chromosome Microdeletions and Alterations of Spermatogenesis.
April 25, 2001
April 28, 2001
May 12, 2001
- 3rd International Meeting on Single Nucleotide Polymorphism and Complex Genome Analysis.SNPs.Some Notable Progress
- A model for chromosome structure during the mitotic and meiotic cell cycles.
- A paradox urgent BRCA genetic testing
- Alpha-fetoprotein Structure and Function.Relevance to Isoforms, Epitopes, and Conformational Variants
- Apoptotic and necrotic cell death induced by death domain receptors
- Appraising organised screening programmes for testing for genetic susceptibility to cancer
- Assembly, Annotation, and Integration of UNIGENE Clusters into the Human Genome Draft
- Cancer risk in mismatch repair gene mutation carriers
- Comparative Genomics of a Conserved Chromosomal Region Associated with a Complex Human Phenotype
- Congenital adrenal hyperplasia-from genetics and biochemistry to clinical practice
- CYP21 mutations and congenital adrenal hyperplasia
- Diagnosis of Japanese patients with HHH syndrome by molecular genetic analysis-a common mutation, R179X
- DNA Breaks in Hypermutating Immunoglobulin Genes.Evidence for a Break-and-Repair Pathway of Somatic Hypermutation
- Early identification of connective tissue disorder
- Epidemiology of myotonic dystrophy in Italy-re-apprisal after genetic diagnosis
- Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families
- Familial cancer database a clinical aide-memoire
- Fertility in Prader-Willi syndrome-a case report with Angelman syndrome in the offspring.
- Gene therapy effectiveness differs for neuronal survival and behavioral performance
- Genetic crossover interference in the human genome
- Genetics of Arterial Prothrombotic Risk States
- Genome Screen for Asthma
- Genotype and phenotype in hereditary nonpolyposis colon cancer a study of families...
- Grounded Theory in Genetic Counseling Research
- Histone H2A variants and the inactive X chromosome-identification of a second macroH2A variant
- How selection shapes variation of the human major histocompatibility complex-a review
- Human rDNA. Evolutionary Patterns within the Genes and Tandem Arrays Derived from Multiple Chromosomes
- Identification of Four Novel Mutations in Classical Menkes Disease and Successful Prenatal DNA Diagnosis
- Increased bone formation and decreased osteocalcin expression induced by reduced Twist dosage in Saethre-Chotzen syndrome
- Interchromosomal effect leading to an increase in aneuploidy in sperm nuclei in a man heterozygous for pericentric inversion (inv 9) and C-heterochromatin
- Ion channels in disease
- Isolation and Characterization of a Novel Gene Containing WD40 Repeats from the Region Deleted in Velo-cardio-facial-DiGeorge Syndrome on Chromosome 22q11
- MECP2 truncating mutations cause histone H4 hyperacetylation in Rett syndrome
- Methylation matters
- Mitochondrial DNA variability in Russians and Ukrainians. Implication to the origin of the Eastern Slavs
- Molecular characterisation of 34 patients with biotinidase deficiency ascertained by newborn screening and family investigation
- Molecular Cloning and Mapping of the Human Nicotinic Acetylcholine Receptor 10 (CHRNA10)
- Participation in Breast Cancer Genetic Counseling The Influence of Educational Level, Ethnic Background, and Risk Perception
- Phylogenetic Network for European mtDNA
- Population-based study of familial medullary thyroid cancer
- Prenatal Diagnosis for Inherited Deafness—What is the Potential Demand
- Report of the ninth international workshop on the molecular biology of human chromosome 21 and Down syndrome
- Report of the sixth international workshop on human chromosome 1 mapping 2000
- Risk factor-gene interaction in carotid atherosclerosis-effect of gene polymorphisms of renin-angiotensin system
- Smith-Lemli-Opitz Syndrome.The First Malformation Syndrome Associated with Defective Cholesterol Synthesis
- The Complete Human Olfactory Subgenome
- The hAT family-a versatile transposon group common to plants, fungi, animals, and man
- The Molecular Basis of X-Linked Spondyloepiphyseal Dysplasia Tarda
- The Prader-Willi Syndrome Imprinting Center Activates the Paternally Expressed Murine Ube3a Antisense Transcript but Represses Paternal Ube3a
- The risk for congenital heart defects in offspring of individuals with congenital heart defects
- The VACTERL association-lessons from the Sonic hedgehog pathway
- Use of an artificial neural network to detect association between a disease and multiple marker genotypes
- Women at risk of ovarian cancer attitudes towards and expectations of the familial ovarian cancer clinic
May 25, 2001
May 31, 2001
June 2, 2001
June 7, 2001
June 13, 2001
June 18, 2001
June 25, 2001
July 3, 2001
July 7, 2001
July 22, 2001
July 26, 2001
July 31, 2001
August 2, 2001
August 4, 2001
August 7, 2001
August 10, 2001
August 15, 2001
August 17, 2001
- A
mutation in SLC11A3 is associated with autosomal dominant hemochromatosis
- Alpha-fetoprotein
Structure and Function. Relevance to Isoforms, Epitopes, and Conformational Variants
- Causes
of haematuria in adult polycystic kidney disease
- Decision
Analysis of Prenatal Testing for Chromosomal Disorders...
- Diagnostic
strategy for familial and sporadic cases of neuropathy associated with 17p11.2
deletion
- DIETARY
AND GENETIC EFFECTS ON LOW-DENSITY LIPOPROTEIN HETEROGENEITY
- DNA
PRIMASES
- Effect
of Down syndrome on the dimensions of dental crowns and tissues
- ETHNIC
DIVERSITY OF CLASS III GENES IN AUTOIMMUNE DISEASE
- Familial
risk of high blood pressure in the Canadian population
- Fibromatoses
in childhood. The desmoid-fibromatosis complex
- First
BRCA1 and BRCA2 Gene Testing Implemented in the Health Care System of Stockholm
- FLIES,
GENES, AND LEARNING
- Folate,
Homocysteine and Neural Tube Defects. An Overview
- Gardner's
syndrome--the importance of early diagnosis-a case report and a review.
- Gene
Expression of Cyclooxygenase in the Aging Heart
- Genes
That Prolong Life
- GENETIC
ASSEMBLY OF THE HEART. Implications for Congenital Heart Disease
- GENETIC
VARIATIONS AND POLYMORPHISMS OF G PROTEIN-COUPLED RECEPTORS. Functional and Therapeutic
Implications
- Genetics
of Arterial Prothrombotic Risk States
- Genetics
of the Neuronal NO-Synthase
- Health
Information Systems and Health Communications. Narrowband and Broadband Technologies
as Core Public Health Competencies
- HUMAN
BRAIN MALFORMATIONS AND THEIR LESSONS FOR NEURONAL MIGRATION
- Identification
of N-Acetyltransferase 2 and CYP2C19 Genotypes for Hair, Buccal Cell Swabs, or
Fingernails Compared With Blood
- Identification
of the gene altered in Berardinelli[#150]Seip congenital lipodystrophy on chromosome
11q13
- Increased
frequency of ATM mutations in breast carcinoma patients with early onset disease
and positive family history
- International
Genetic Epidemiology Society. Commentary on Darkness in El Dorado by Patrick Tierney
- Maternal
and paternal age at delivery, birth order, and risk of childhood onset type 1
diabetes-population based cohort study
- MATERNAL
CARE, GENE EXPRESSION, AND THE TRANSMISSION OF INDIVIDUAL DIFFERENCES IN STRESS
REACTIVITY ACROSS GENERATIONS
- Mitotic
recombination effects homozygosity for NF1 germline mutations in neurofibromas
- MOLECULAR
BASIS OF ETHNIC DIFFERENCES IN DRUG DISPOSITION AND RESPONSE
- MOLECULAR
REGULATION OF LUNG DEVELOPMENT
- NEURODEGENERATIVE
TAUOPATHIES
- NEW
DNA SEQUENCING METHODS
- Pharmacogenomics
of Cystic Fibrosis
- PHARMACOGENOMICS.
Unlocking the Human Genome for Better Drug Therapy
- Predictors
of Healthy Brain Aging
- Prevalence
and patterns of presentation of genetic disorders in a pediatric emergency department.
- Sites
of interest on the World Wide Web - Drug Information
- Sites
of interest on the World Wide Web—edited by Rick Neubig
- SOMATIC
GENE THERAPY IN THE CARDIOVASCULAR SYSTEM
- STEM
CELL BIOENGINEERING
- Teratogen
update - Inorganic arsenic
- THE
DEVELOPMENTAL BIOLOGY OF BRAIN TUMORS
- The
genetic basis of renal epithelial tumors-advances in research and its impact on
prognosis and therapy
- The
prospect of gene therapy for prostate cancer-update on theory and status
- X-LINKED
LYMPHOPROLIFERATIVE DISEASE. A Progressive Immunodeficiency
August 22, 2001
August 25, 2001
August 29, 2001
August 31, 2001
September 5, 2001
September 8, 2001
September 11, 2001
September 14, 2001
September 17, 2001
September 20, 2001
- 10th
International HUGO Mutation Database Initiative Meeting, 19 April 2001, Edinburgh,
Scotland
- 30th
Annual Meeting of the Child Neurology Society.Abstracts.Genetics, Dysgenesis,
and Metabolic Disease
- 7-Dehydrocholesterol–dependent
proteolysis of HMG-CoA reductase suppresses sterol biosynthesis in a mouse model
of Smith-Lemli-Opitz-RSH syndrome
- Cancer
genetics in oncology practice
- Congenital
lung disease. A plea for clear thinking and clear nomenclature
- Fine
mapping and single nucleotide polymorphism association results of candidate genes
for asthma and related phenotypes
- Genotype-phenotype
comparison of the Swiss malignant hyperthermia population
- Her-2(neu)
and Breast Cancer
- Lysosomal
multienzyme complex-biochemistry, genetics, and molecular pathophysiology.
- Malignant
hyperthermia
- Molecular
genetics of mucopolysaccharidosis type IIIA and IIIB.Diagnostic, clinical, and
biological implications
- Mutations
in severe combined immune deficiency (SCID) due to JAK3 deficiency
- Parkinson's
disease-clinical features, epidemiology and genetics
- Pediatric
oncology and the Internet
- Psoriatic
arthritis-clinical aspects, genetics, and the role of T cells
- RB1
genetic testing as a clinical service. A follow-up study
- Screening
for Wilms tumor and hepatoblastoma in children with Beckwith-Wiedemann syndromes.
September 22, 2001
September 25, 2001
September 28, 2001
September 30, 2001
October 3, 2001
October 5, 2001
October 9, 2001
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