Works matching IS 09646906 AND DT 1992 AND VI 1 AND IP 7
Results: 33
A new VNTR-type RFLP probe (ChdTC-114) on chromosome 20p (D20S72).
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 554
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- Article
A new VNTR-type RFLP probe (λTM-18) on chromosome 1 (D1S157).
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 554
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- Article
Dinucleotide repeat polymorphism in the human thyroid hormone receptor α gene (THRA1) on chromosome 17.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 553
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- Article
Dinucleotide repeat polymorphism at the D18S19 locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 553
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- Article
Dinucleotide repeat polymorphism between the human C4BPA and C4BPB gene loci (1q32).
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 552
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- Article
An EcoRI RFLP at the human insulin-like growth factor binding protein 2 gene (IGFBP2).
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 552
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- Article
A chromosome 19 CA-dinucleotide repeat polymorphism.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 551
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- Article
An Sphl polymorphism at the ZNF22 locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 551
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- Article
An Sphl polymorphism at the vinculin locus (VCL).
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 550
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- Article
Taql polymorphisms at the annexin VIII locus (ANX8).
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 550
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- Article
Dinucleotide repeat polymorphism at the D9SI47E locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 549
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- Article
Dinucleotide repeat polymorphism at the D7S476 locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 549
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- Article
Erratum.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 558
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Author index.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 557
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- Article
A new VNTR-type RELP probe (ChdTC-15) on chromosome 12 (D12S65).
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 555
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- Article
Dinucleotide repeat polymorphisms at the D11S439 and HBB loci.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 548
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- Publication type:
- Article
Dinucleotide repeat polymorphisms (D21S223 and D21S224) at 21q22.1.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 547
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- Article
A novel frame-shift mutation in exon 4 of the cystic fibrosis gene (435insA) demonstrates the ambiguity of restriction analysis for mutation screening.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 545
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- Article
CFTR nonsense mutations G542X and W1282X associated with severe reduction of CFTR mRNA in nasal epithelial cells.
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- Human Molecular Genetics, 1992, v. 1, n. 7, p. 542
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- Article
Mismatch PCR: a rapid method to screen for the Pro → Leu mutation in the lipoprotein lipase (LPL) gene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 541
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- Article
Oligonucleotide probes for the analysis of specific repetitive DNA sequences by fluorescence in situ hybridization.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 535
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- Article
Genomic organization of a cDNA (QM) demonstrating an altered mRNA level in nontumorigenic Wilms' microcell hybrid cells and its localization to Xq28.
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- Human Molecular Genetics, 1992, v. 1, n. 7, p. 529
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- Article
The genomic structure of the human skeletal muscle sodium channel gene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 521
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- Article
Detection of a nonsense mutation in the dystrophin gene by multiple SSCP.
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- Human Molecular Genetics, 1992, v. 1, n. 7, p. 517
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Segregation of the fragile X mutation from an affected male to his normal daughter.
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- Human Molecular Genetics, 1992, v. 1, n. 7, p. 511
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Expression of four alternative dystrophin transcripts in brain regions regulated by different promoters.
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- Human Molecular Genetics, 1992, v. 1, n. 7, p. 505
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Androgen receptor gene mutations identified by SSCP in fourteen subjects with androgen insensitivity syndrome.
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- Human Molecular Genetics, 1992, v. 1, n. 7, p. 497
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Autosomal dominant branchio-oto-renal syndrome—localization of a disease gene to chromosome 8q by linkage in a Dutch family.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 491
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- Article
Characterization of a 1.0 Mb YAC contig spannning two chromosome breakpoints related to Menkes disease.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 483
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- Article
The large non-collagenous domain (NC-1) of type VII collagen is amino-terminal and chimeric. Homology to cartilage matrix protein, the type III domains of fibronectin and the A domains of von Willebrand factor.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 475
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Unstable DNA may be responsible for the incomplete penetrance of the myotonic dystrophy phenotype.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 467
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Mutations in the candidate gene for Norrie disease.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 461
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- Article
Cystic fibrosis mice have arrived!
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 7, p. 459
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- Article