EcoRV RFLP of the desmin (DES) gene and Mspl RFLP of the villin (VIL1) gene on human chromosome 2.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 448
- By:
- Publication type:
- Article
Works matching IS 09646906 AND DT 1992 AND VI 1 AND IP 6
Results: 33
1
2
Author index.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 457
- Publication type:
- Article
3
Dinucleotide repeat polymorphism at the D21S258 locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 449
- By:
- Publication type:
- Article
4
Four dinucleotide repeat polymorphisms on chromosome 9 (D9S143–146).
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 447
- By:
- Publication type:
- Article
5
G27X: a novel mutation in exon 2 of the CF gene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 445
- By:
- Publication type:
- Article
6
Deletion in the prion protein gene in a demented patient.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 443
- By:
- Publication type:
- Article
7
A Serine to proline substitution (S1255P) in the second nucleotide binding fold of the cystic fibrosis gene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 441
- By:
- Publication type:
- Article
8
Detection of novel and rare mutations in exon 4 of the cystic fibrosis gene by SSCP.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 439
- By:
- Publication type:
- Article
9
Identification of genes using oligonucleotides corresponding to splice site consensus sequences.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 433
- By:
- Publication type:
- Article
10
Characterization of mutations in phenotypic variants of hypoxanthine phosphoribosyltransferase deficiency.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 427
- By:
- Publication type:
- Article
11
Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11–13) by YAC cloning and FISH analysis.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 417
- By:
- Publication type:
- Article
12
Autosomal dominant Retinitis Pigmentosa (adRP): exclusion of a gene from three mapped loci provides evidence for the existence of a fourth locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 411
- By:
- Publication type:
- Article
13
Characterization of the human HOX 7 cDNA and identification of polymorphic markers.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 407
- By:
- Publication type:
- Article
14
Minisatellite variant repeat (MVR) mapping: analysis of ‘null’ repeat units at D1S8.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 401
- By:
- Publication type:
- Article
15
DNA methylation represses FMR-1 transcription in fragile X syndrome.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 397
- By:
- Publication type:
- Article
16
Rapid and simultaneous detection of multiple mutations by pooled and multiplex single nucleotide primer extension: application to the study of insulin-responsive glucose transporter and insulin receptor mutations in non-insulindependent diabetes.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 391
- By:
- Publication type:
- Article
17
Inactivation of both APC alleles in an early stage of colon adenomas in a patient with familial adenomatous polyposis (FAP).
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 387
- By:
- Publication type:
- Article
18
A molecular deletion map of the Y chromosome long arm defining X and autosomal homologous regions and the localisation of the HYA locus to the proximal region of the Yq euchromatin.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 379
- By:
- Publication type:
- Article
19
Human CC10, the homologue of rabbit uteroglobin: genomic cloning, chromosomal localization and expression in endometrial cell lines.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 371
- By:
- Publication type:
- Article
20
Long-term persistence of plasmid DNA and foreign gone expression in mouse muscle.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 363
- By:
- Publication type:
- Article
21
Genome mapping and sequencing 1992: a meeting report.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 359
- By:
- Publication type:
- Article
22
Dinucleotide repeat polymorphism at the topoisomerase (DNA) I pseudogene 2 (TOPIP2).
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 455
- By:
- Publication type:
- Article
23
Dinucleotide repeat polymorphism at the D5S253 locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 455
- By:
- Publication type:
- Article
24
Dinucleotide repeat polymorphism at the D19S206 locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 454
- By:
- Publication type:
- Article
25
Dinucleotide repeat polymorphism at the D1S182 locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 454
- By:
- Publication type:
- Article
26
SSCP polymorphism in the human hepatic triglyceride lipase (LIPC) gene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 453
- By:
- Publication type:
- Article
27
Alu polymorphism in the human type I Keratin (KRT14) gene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 453
- By:
- Publication type:
- Article
28
A microsatellite polymorphic probe on chromosome 3p: λLIB12–2CATT (D3S1244).
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 452
- By:
- Publication type:
- Article
29
(CA)n-dinucleotide repeat polymorphism at the locus for the alpha2C adrenergic receptor (ADRA2C) on 4p16.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 452
- By:
- Publication type:
- Article
30
Taql and Bsu361 polymorphisms in the human glycoprotein Ibα gene (GPIBα).
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 451
- By:
- Publication type:
- Article
31
Insertion/deletion polymorphism at D19S95 associated with the myotonic dystrophy CTG repeat.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 451
- By:
- Publication type:
- Article
32
Dinucleotide repeat polymorphism at the RBP3 locus in chromosome band 10q11.2.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 450
- By:
- Publication type:
- Article
33
Single base polymorphism at −511 in the human interleukin-1β gene (IL1β).
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 450
- By:
- Publication type:
- Article