The gene encoding the palmitoylated erythrocyte membrane protein, p55, originates at the CpG island 3′ to the factor VIII gene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 97
- By:
- Publication type:
- Article
Works matching IS 09646906 AND DT 1992 AND VI 1 AND IP 2
Results: 27
1
2
Isolation and characterization of a novel gene with differential expression in benign and malignant human breast tumours.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 91
- By:
- Publication type:
- Article
3
The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 83
- By:
- Publication type:
- Article
4
Identification and developmental expression of the Xenopus laevis cystic fibrosis transmembrane conductance regulator gene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 77
- By:
- Publication type:
- Article
5
An autosomal homologue of the choroideremia gene colocalizes with the usher syndrome type II locus on the distal part of chromosome 1q.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 71
- By:
- Publication type:
- Article
6
Author index.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 145
- Publication type:
- Article
7
A polymorphic dinucleotide repeat in intron 2 of the human cystatin-C gene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 143
- By:
- Publication type:
- Article
8
A dinucleotide repeat polymorphism at the D4S127 locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 142
- By:
- Publication type:
- Article
9
Probe D16S273 detects a Pstl RFLP with 8 alleles.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 142
- By:
- Publication type:
- Article
10
Dinucleotide repeat polymorphism for the hexabrachion gene (HXB) on chromosome 9q32–34.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 141
- By:
- Publication type:
- Article
11
A new highly polymorphic dinucleotide (CT)n repeat polymorphism D1S158 on chromsome 1q isolated by microdissection.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 141
- By:
- Publication type:
- Article
12
Dinucleotide repeat in the human mitochondrial D-loop.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 140
- By:
- Publication type:
- Article
13
A series of hypervariable minisatellites at the D7S464 locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 140
- By:
- Publication type:
- Article
14
Dinucleotide repeat polymorphism at the D15S11 locus in the Angelman/Prader—Willi region (AS/PWS) of chromosome 15.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 139
- By:
- Publication type:
- Article
15
Dinucleotide repeat polymorphism at the hormone sensitive lipase (LIPE) locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 139
- By:
- Publication type:
- Article
16
A polymorphic dinucleotide repeat in intron 1 of the human tissue plasminogen activator gene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 138
- By:
- Publication type:
- Article
17
Dinucleotide repeat polymorphism at the D1S167 locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 138
- By:
- Publication type:
- Article
18
Tetranucleotide repeat polymorphism at the human thyroid peroxidase (hTPO) locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 137
- By:
- Publication type:
- Article
19
Dinucleotide repeat polymorphism at the human cardiac β-myosin heavy chain gene (HMSYHCO1) locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 136
- By:
- Publication type:
- Article
20
Two chromosome 7 dinucleotide repeat polymorphisms at gene loci epidermal growth factor receptor (EGFR) and proα2 (1) collagen (COL1A2).
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 135
- By:
- Publication type:
- Article
21
Isolation and characterization of 19 dinucleotide repeat polymorphisms on chromosome 3p.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 131
- By:
- Publication type:
- Article
22
De novo mutation in the COL4A5 gene converting glycine 325 to glutamic acid in Alport syndrome.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 127
- By:
- Publication type:
- Article
23
A new missense mutation (R1283M) in exon 20 of the cystic fibrosis transmembrane conductance regulator gene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 123
- By:
- Publication type:
- Article
24
An optimized Alu-PCR primer pair for human-specific amplification of YACs and somatic cell hybrids.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 121
- By:
- Publication type:
- Article
25
A male with two contiguous inactivation centers on a single X chromosome: study of X inactivation and XIST expression.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 115
- By:
- Publication type:
- Article
26
Characterisation of a new rare fragile site easily confused with the fragile X.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 111
- By:
- Publication type:
- Article
27
Characterization of a 4.8kb transcript from the Duchenne muscular dystrophy locus expressed in Schwannoma cells.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 103
- By:
- Publication type:
- Article