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