| Improved Risk Assessment for
Insulin-Dependent Diabetes
mellitus by Analysis of Amino
Acids in HLA-DQ and DRB1 Loci |
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| Author Index Vol. 2, 1994 |
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| The Second Year of the European Journal of Human Genetics |
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| A Systematic Search for
Uniparental Disomy in Carriers of
Chromosome Translocations |
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| Strong Founder Effect for the
Fragile X Syndrome in Sweden |
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| Transforming Growth Factor
Alpha: A Modifying Locus for
Nonsyndromic Cleft Lip with or
without Cleft Palate? |
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| Analysis of the Molecular
Variance at the Phenylalanine
Hydroxylase (PAH) Locus |
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| A European Research Conference
on the Inherited Disorders and
Their Genes in Different European
Populations |
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✓ |
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European populations |
| Report of ESHG Satellite Meeting:
EU Concerted Action on Genetic
Services in Europe (CAGSE) |
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| Announcements |
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| Hunting the Hemochromatosis
Gene: Progress and Problems |
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| The X Inactivation Centre and
X Chromosome Imprinting |
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| Mapping of Friedreich's Ataxia
Locus by Identification of
Recombination Events in Patients
Homozygous by Descent |
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| Parental Imprinting of Human Chromosome Region 11p15.3-pter Involved in the Beckwith-Wiedemann Syndrome and Various Human Neoplasia |
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| DNA Diagnostics of the Marfan
Syndrome: Application of
Amplifîable Polymorphie Markers |
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| Announcement |
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| Announcements |
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| Further Localization of the Gene
for Hereditary Paragangliomas
and Evidence for Linkage in
Unrelated Families |
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| Mapping of Microsatellite Markers
in the Alagille Region and
Screening of Microdeletions by
Genotyping 23 Patients |
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| Announcements |
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| Universal Screening for
Hemoglobinopathies Using
High-Performance Liquid
Chromatography: Clinical Results
of 2.2 Million Screens |
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| Subject Index Vol. 2, 1994 |
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| Origins of Hyperphenylalaninemia
in Israel |
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| Limited Expansion of the (CAG)n
Repeat of the Huntington Gene:
A Premutation (?) |
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| A Deletion Hybrid Breakpoint Map
of the Chromosomal Region
13q14-q21 Orders 19 Genetic
Markers in 10 Intervals |
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| Difference in Frequencies of the
Cystic Fibrosis Alleles, ∆F508 and
W1282X, between Carriers and
Patients |
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| Counselling following Diagnosis
of Fetal Abnormality:
A Comparison between German,
Portuguese and UK Geneticists |
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| Assignment of Granular Corneal
Dystrophy Groenouw Type I
(CDGG1 ) to Chromosome 5q |
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| European Gene Mapping Project
(EUROGEM): Genetic Maps based
on the CEPH reference families |
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✓ |
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|
European Gene Mapping Project |
| The 8993 mtDNA Mutation:
Heteroplasmy and Clinical
Presentation in Three Families |
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| A Study of X Chromosome
Activity in Two Incontinentia
pigmenti Families with Probable
Linkage to Xq28 |
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| Mutations in the Muscle Sodium
Channel Gene (SCN4A) in 13 French
Families with Hyperkalemic Periodic
Paralysis and Paramyotonia
Congenita: Phenotype to Genotype
Correlations and Demonstration of the
P |
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| Transition from Normal to
Premutated Alleles in
Fragile X Syndrome Results
from a Multistep Process |
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| Heterogeneity and Low Detection
Rate of RET Mutations in
Hirschsprung Disease |
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| Frequent Constitutional C to T
Mutations in CGA-Arginine
Codons in the RB1 Gene Produce
Premature Stop Codons in
Patients with Bilateral (Hereditary)
Retinoblastoma |
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| Contents Vol. 2, 1994 |
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