European Journal of Human Genetics - 1997

126 articles | Last updated: 2025-12-03 14:12:56
Caucasian
0
White
0
European
1
Other
1
Article Title Cauc. White Euro. Other Phrases Used
T A T A T A T A
Prenatal Diagnosis in Germany
Preface: Three Principles
Prenatal Diagnosis in Finland
Prenatal Diagnosis in the Netherlands
Genetic Services in Belgium
Genetic Services in Finland
Genetic Services in Ireland
Genetic Services in Italy
Genetic Services in Latvia
Contents Vol. 5, Suppl. 1, 1997
Prenatal Diagnosis in France
Prenatal Diagnosis in Italy
Prenatal Diagnosis in Portugal
Prenatal Diagnosis in the United Kingdom - An Overview
Medical Genetic Services in 31 Countries: An Overview
Genetic Services in Croatia
Proceedings of the EUCROMIC Workshop on Prenatal Diagnosis
Prenatal Diagnosis in Luxembourg
Contents Vol. 5, Suppl. 2, 1997
DNA Diagnosis and the Emergence of Cancer Genetic Services in European Health Care
Genetic Services in Austria
Genetic Services in Bulgaria
Genetic Services in Denmark
Genetic Services in Norway
Genetic Services in Serbia
Prenatal Diagnosis in Spain
Genetic Services in the Czech Republic
Genetic Services in Lithuania
Genetic Services in Russia
Genetic Services in Switzerland
Prenatal Diagnosis in Sweden: Organisation and Current Issues
Genetic Services in Hungary
Genetic Services in Israel
Genetic Services in The Netherlands
Genetic Services in Romania
Genetic Services in Spain
Genetic Services in the Ukraine
Data Annex
Prenatal Diagnosis Services in Greece
Genetic Services in Cyprus
Genetic Services in France
Genetic Services in Greece
Genetic Services in Portugal
Genetic Services in Slovenia
Genetic Services in Sweden
Genetic Services in Turkey
Prenatal Diagnosis in Belgium
Prenatal Diagnosis in Denmark
Prenatal Diagnosis in Norway
Prenatal Diagnosis in Switzerland
Clinical Stage, Prostate-Specific Antigen and Gleason Grade to Predict Extracapsular Disease or Nodal Metastasis in Men with Newly Diagnosed, Previously Untreated Prostate Cancer
Dimensions of Quality in Genetic Services - An Ethical Comment
Genetic Services in Germany
Genetic Services in Poland
Genetic Services in the United Kingdom
Editorial
Non-Participation in Predictive Testing for Huntington's Disease: Individual Decision-Making, Personality and Avoidant Behaviour in the Family
Erythrocyte Glucose-6-Phosphate Dehydrogenase Deficiency in Poland - a Study on the 563 and 1311 Mutations of the G6PD Gene
Altered mRNA Expression due to Insertion or Substitution of Thymine at Position +3 of Two Splice-Donor Sites in the Androgen Receptor Gene
The Meiotic Segregation Pattern of a Reciprocal Translocation t(10;12)(q26.1; p13.3) by Fluorescence in situ Hybridization Sperm Analysis
Assignment and Ordering of Twenty-Three Unique NotI-Linking Clones Containing Expressed Genes Including the Guanosine 5'-Monophosphate Synthetase Gene to Human Chromosome 3
A YAC Contig Spanning the Blepharophimosis-Ptosis- Epicanthus inversus Syndrome and Propionic Acidemia Loci
Refined Subchromosomal Location of 21 Expressed Sequence Tags from Unknown Genes at Region 11p15
mtDNA Haplotype Analysis in Finnish Families with Leber Hereditary Optic Neuroretinopathy
Integrated Radiation Hybrid and Yeast Artificial Chromosome Map of Chromosome 9p
A Xanthomatosis-Susceptibility Gene May Exist in a Syrian Family with Familial Hypercholesterolemia
Genoa Meeting / Announcement
Contents Vol. 5, 1997
Two New Mutations in the Glucose-6-Phosphatase Gene Cause Glycogen Storage Disease in Hungarian Patients
Estimating Recessive Disease Allele Frequency Based on Genetic Maps
Y-Chromosome STR Loci in Sardinia and Continental Italy Reveal Islander-Specific Haplotypes
FMR1 Premutation Allele (CGG)(81) Is Stable in Mice
Genetic Variation at the apoB 3' Hypervariable Region in a Serbian Population
Refined Mapping of a Gene for Autosomal Dominant Progressive Sensorineural Hearing Loss (DFNA5) to a 2-cM Region, and Exclusion of a Candidate Gene That Is Expressed in the Cochlea
Could the 185delAG BRCA1 Mutation Be an Ancient Jewish Mutation?
Somatic Mosaicism in Fanconi Anemia: Molecular Basis and Clinical Significance
Mutations in Hirschsprung Disease: When Does a Mutation Contribute to the Phenotype
Relationship between Mutation Genotype and Biochemical Phenotype in a Heterogeneous Spanish Phenylketonuria Population
Three Novel Point Mutations in the Keratinocyte Transglutaminase (TGK) Gene in Lamellar Ichthyosis: Significance for Mutant Transcript Level, TGK Immunodetection and Activity
Endothelin-3 Gene Mutations in Isolated and Syndromic Hirschsprung Disease
Characterisation of X;17(q12;p13) Translocation Breakpoints in a Female Patient with Hypomelanosis of Ito and Choroid Plexus Papilloma
Mapping of Papillon-Lefèvre Syndrome to the Chromosome 11q14 Region
Tetrasomy 18p Caused by Paternal Meiotic Nondisjunction
BOR and BO Syndromes Are Allelic Defects of EYA1
Genetic Analysis by Chromosome Sorting and Painting: Phylogenetic and Diagnostic Applications
A Single-Base Deletion in the 3'-Coding Region of Glycogen-Debranching Enzyme Is Prevalent in Glycogen Storage Disease Type IIIA in a Population of North African Jewish Patients North African Jewish
The Mouse Necdin Gene Is Expressed from the Paternal Allele Only and Lies in the 7C Region of the Mouse Chromosome 7, a Region of Conserved Synteny to the Human Prader-Willi Syndrome Region
Further Delineation of the Critical Region for Noonan Syndrome on the Long Arm of Chromosome 12
Juvenile and Adult Hemochromatosis Are Distinct Genetic Disorders
Identification and Characterization of a Novel Member of the EXT Gene Family, EXTL2
Mitochondrial Sequence Variants in Patients with Schizophrenia
Author Index Vol. 5, 1997
Nephropathie Cystinosis (CTNS-LSB): Construction of a YAC Contig Comprising the Refined Critical Region on Chromosome 17p13
Characterisation of Five Missense Mutations in the Cystathionine Beta-Synthase Gene from Three Patients with B(6)-Nonresponsive Homocystinuria
Mitochondrial DNA and Y Chromosome-Specific Polymorphisms in the Seminole Tribe of Florida
Uniparental Disomy in Cartilage-Hair Hypoplasia
Relationship Estimation in Affected Sib Pair Analysis of Late-Onset Diseases
The Fragile X CGG Repeat Shows a Marked Level of Instability in Hereditary Non-Polyposis Colorectal Cancer Patients
Chromosomal Localization of the Adrenoleukodystrophy-Related Gene in Man and Mice
Osteogenesis imperfecta Phenotypes Resulting from Serine for Glycine Substitutions in the α2(I) Collagen Chain
Announcements
Refined Mapping of the Cohen Syndrome Gene by Linkage Disequilibrium
Deletion of 11 Amino Acids in Tuberin Associated with Severe Tuberous Sclerosis Phenotypes: Evidence for a New Essential Domain in the First Third of the Protein
Trisomy First, Translocation Second, Uniparental Disomy and Partial Trisomy Third: A New Mechanism for Complex Chromosomal Aneuploidy
Development and Clinical Application of an Innovative Fluorescence in situ Hybridization Technique Which Detects Submicroscopic Rearrangements Involving Telomeres
Association of Extracolonic Manifestations of Familial Adenomatous Polyposis with Acetylation Phenotype in a Large FAP Kindred
Linkage of DFNB1 to Non-Syndromic Neurosensory Autosomal-Recessive Deafness in Mediterranean Families
A Single-Tube PCR Test for the Diagnosis of Angelman and Prader-Willi Syndrome Based on Allelic Methylation Differences at the SNRPN Locus
Mapping of the X-Breakpoint Involved in a Balanced X;12 Translocation in a Female with Mild Mental Retardation
CFTR Gene Mutations in Adults with Disseminated Bronchiectasis
A Number of Schizencephaly Patients Including 2 Brothers Are Heterozygous for Germline Mutations in the Homeobox Gene EMX2
Announcements
Werner Syndrome: Characterization of Mutations in the WRN Gene in an Affected Family
Transient Neonatal Diabetes mellitus in a Child with invdup(6)(q22q23) of Paternal Origin
Subject Index Vol. 5, 1997
Announcements
Human and Clinical Cytogenetics: Origins, Evolution and Impact
A Chronic GM(2) Gangliosidosis Variant with a HEXA Splicing Defect: Quantitation of HEXA mRNAs in Normal and Mutant Fibroblasts
Refined Localisation of the Genes for Nebulin and Titin on Chromosome 2q Allows the Assignment of Nebulin as a Candidate Gene for Autosomal Recessive Nemaline Myopathy
Quality Guidelines and Standards for Genetic Laboratories/Clinics in Prenatal Diagnosis on Fetal Samples Obtained by Invasive Procedures
A Molecular Survey of Phenylketonuria in Iceland: Identification of a Founding Mutation and Evidence of Predominant Norse Settlement Norse settlement
Haemoglobin D-Ouled Rabah among the Mozabites: A Relevant Variant to Trace the Origin of Berber-Speaking Populations
Mapping of the Tyrosine Kinase Receptors trkA (NTRK1), trkB (NTRK2) and trkC (NTRK3) to Human Chromosomes 1q22,9q22 and 15q25 by Fluorescence in situ Hybridization
Linkage Analysis in 16 Families with Incontinentia pigmenti
Editorial
Lack of Hemizygosity for the Insulin-Like Growth Factor I Receptor Gene in a Quantitative Study of 33 Silver Russell Syndrome Probands and Their Families