| Deletion and Insertion Mutations
in Short Tandem Repeats in the
Coding Regions of Human Genes |
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| DNA-Based Presymptomatic
Diagnosis for the
von Hippel-Lindau Disease by
Linkage Analysis |
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| Detection of Homozygosity by Descent |
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| No Evidence for Segregation Distortion of Cystic Fibrosis Alleles among Sibs of Cystic Fibrosis Patients |
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| About Our Journal and
Our Society |
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| Contents Vol. 3,1995 |
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| A Search for Uniparental Disomy
in Carriers of Supernumerary
Marker Chromosomes |
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| DNA Polymorphisms in the
Lactase Gene |
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| Simultaneous Formation of inv
dup(15) and dup(15q) in a Girl with
Developmental Delay: Origin of
the Abnormal Chromosomes |
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| Yeast Artificial Chromosome Cloning
of the Xq13.3-q21.31 Region and Fine
Mapping of a Deletion Associated with
Choroideremia and Nonspecific
Mental Retardation |
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| Presence of an IDS-Related Locus
(IDS2) in Xq28 Complicates the
Mutational Analysis of Hunter
Syndrome |
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| Can Nucleated Erythrocytes
Found in Maternal Venous
Blood Be Used in the
Noninvasive Prenatal
Diagnosis of Fetal
Chromosome Abnormalities? |
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| Exclusion Mapping of Classical Late Infantile Neuronal Ceroid Lipofuscinosis (Jansky-Bielschowsky Disease, CLN2) |
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| A Limited Genomic Region
Contains the Human REG and
REG-Related Genes |
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| Molecular Genetics of the
Human Chondrodysplasias -1995 |
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| Announcement |
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| Author Index Vol. 3,1995 |
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| Subject Index Vol. 3,1995 |
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| Placement and Refined Mapping of
Established and New Markers on
Human Chromosome 11q Using a
Small Panel of Somatic Cell Hybrids |
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| Ataxia-Telangiectasia:
Closer to Unraveling the Mystery |
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| DNA Forensic Science 1995 |
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| Expression of the Human Dp 71 (Apo-Dystrophin-1 ) Gene from a 760-kb DMD-YAC Transferred to Mouse Cells |
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| Announcements |
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| Linkage Disequilibrium between the
Expanded (CAG)(n) Repeat and an Allele
of the Adjacent (CCG)(n) Repeat in
Huntington's Disease Patients of
Greek Origin |
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✓ |
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Greek Origin |
| Characterization of Phenylketonuria Alleles in the Italian Population |
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| The Genetic Background of
Craniosynostosis Syndromes |
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| Announcements |
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| Seeding of YACs over Regions
1q41-q42.3 and 11q14.3-q23 with
Microdissection Clones |
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| Conference Report |
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| The Third Year of the EJHG |
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| Heterozygote Screening for Cystic
Fibrosis |
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| A Provisional Transcript Map of
the Spinal Muscular Atrophy
(SMA) Critical Region |
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| Isolation of Microsatellites from the
Spinal Muscular Atrophy (SMA)
Candidate Region on Chromosome 5q
and Linkage Analysis in Spanish SMA
Families |
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| An Integrated Map of Human Chromosome 13 Allowing Regional Localization of Genetic Markers |
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| Reply |
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| Evidence of Linkage between Susceptibility to Multiple Sclerosis and HLA-Class II Loci in Italian Multiplex Families |
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| Mapping of the Spinal Muscular
Atrophy (SMA) Gene to a 750-kb
Interval Flanked by Two New
Microsatellites |
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| Cosmid Contigs Spanning 9q34
Including the Candidate Region
forTSCI |
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| Cosmid Contigs from the
Tuberous Sclerosis Candidate
Region on Chromosome 9q34 |
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| Identification of Two New
Mutations in Congenital
Erythropoietic Porphyria |
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| Medical Genetics in Israel |
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| A Genetic Map of Chromosome 11q, Including the Atopy Locus |
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| Convergent Myotonie Dystrophy (DM) Haplotypes: Potential Inconsistencies in Human Disease Gene Localization |
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| A Quality Control Study of CFTR
Mutation Screening in 40
Different European Laboratories |
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✓ |
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European |
| Complete Spectrum of PAH
Mutations in Tataria:
Presence of Slavic, Turkic and
Scandinavian Mutations |
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✓ |
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Slavic, Turkic and Scandinavian |
| Do Basque- and Caucasian-
Speaking Populations Share
Non-Indo-European Ancestors? |
✓ |
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✓ |
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Basque |
| Announcements |
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| Frequent Occurrence of the CFTR
Intron 8 (TG)n 5T Allele in Men with
Congenital Bilateral Absence of the Vas Deferens |
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| Direct Detection of Non-Random
X Chromosome Inactivation by
Use of a Transcribed
Polymorphism in the XIST Gene |
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| Hypothesis: Patient with Possible
Disturbance in Programmed Cell
Death |
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| Opening Address |
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| Widukind Lenz |
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| Physical Mapping Evidence for a Duplicated Region on Chromosome 10qter Showing High Homology with the Facioscapulohumeral Muscular Dystrophy Locus on Chromosome 4qter |
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| CRASH Syndrome: Clinical Spectrum of Corpus Callosum Hypoplasia, Retardation, Adducted Thumbs, Spastic Paraparesis and Hydrocephalus Due to Mutations in One Single Gene, L1 |
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