Works matching IS 09646906 AND DT 1992 AND VI 1 AND IP 6
Results: 33
Author index.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 457
- Publication type:
- Article
Dinucleotide repeat polymorphism at the D21S258 locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 449
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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
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- Article
Four dinucleotide repeat polymorphisms on chromosome 9 (D9S143–146).
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 447
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G27X: a novel mutation in exon 2 of the CF gene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 445
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Deletion in the prion protein gene in a demented patient.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 443
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- Article
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
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- Article
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
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Identification of genes using oligonucleotides corresponding to splice site consensus sequences.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 433
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Characterization of mutations in phenotypic variants of hypoxanthine phosphoribosyltransferase deficiency.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 427
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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
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- Article
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
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Characterization of the human HOX 7 cDNA and identification of polymorphic markers.
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- Human Molecular Genetics, 1992, v. 1, n. 6, p. 407
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- Article
Minisatellite variant repeat (MVR) mapping: analysis of ‘null’ repeat units at D1S8.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 401
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- Article
DNA methylation represses FMR-1 transcription in fragile X syndrome.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 397
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- Article
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
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- Publication type:
- Article
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
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- Publication type:
- Article
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
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- Article
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
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- Article
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
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Genome mapping and sequencing 1992: a meeting report.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 359
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- Article
Dinucleotide repeat polymorphism at the topoisomerase (DNA) I pseudogene 2 (TOPIP2).
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 455
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- Article
Dinucleotide repeat polymorphism at the D5S253 locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 455
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Dinucleotide repeat polymorphism at the D19S206 locus.
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- Human Molecular Genetics, 1992, v. 1, n. 6, p. 454
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Dinucleotide repeat polymorphism at the D1S182 locus.
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- Human Molecular Genetics, 1992, v. 1, n. 6, p. 454
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SSCP polymorphism in the human hepatic triglyceride lipase (LIPC) gene.
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- Human Molecular Genetics, 1992, v. 1, n. 6, p. 453
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Alu polymorphism in the human type I Keratin (KRT14) gene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 453
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A microsatellite polymorphic probe on chromosome 3p: λLIB12–2CATT (D3S1244).
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 452
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- Publication type:
- Article
(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
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Taql and Bsu361 polymorphisms in the human glycoprotein Ibα gene (GPIBα).
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 451
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- Publication type:
- Article
Insertion/deletion polymorphism at D19S95 associated with the myotonic dystrophy CTG repeat.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 451
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Dinucleotide repeat polymorphism at the RBP3 locus in chromosome band 10q11.2.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 450
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- Publication type:
- Article
Single base polymorphism at −511 in the human interleukin-1β gene (IL1β).
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 450
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- Article