Works matching IS 09646906 AND DT 1992 AND VI 1 AND IP 5
Results: 26
A Rsal polymorphism in the ERCC2 locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 5, p. 355
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- Article
Dinucleotide repeat polymorphism at the GABAA receptor α5 (GABRA5) locus at chromosome 15q11-q13.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 5, p. 348
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- Article
Improving the polymorphism content of the 3′ UTR of the human IGF2R gene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 5, p. 347
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A 3′ consensus splice mutation in the human dystrophin gene detected by a screening for intra-exonic deletions.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 5, p. 345
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- Article
Detection of ABO blood group polymorphism by denaturing gradient gel electrophoresis.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 5, p. 341
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- Article
Mutation analysis of the iduronate-2-sulfatase gene in patients with mucopolysaccharidosis type II (Hunter syndrome).
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 5, p. 335
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- Article
Isolation and mapping to 17p12 – 13 of the human homologous of the murine growth arrest specific Gas-3 gene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 5, p. 331
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- Article
D20S19, linked to low voltage EEG, benign neonatal convulsions, and Fanconi anaemia, maps to a region of enhanced recombination and is localized between CpG islands.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 5, p. 325
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- Article
Isolation of human minisatellite loci detected by synthetic tandem repeat probes: direct comparison with cloned DNA fingerprinting probes.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 5, p. 319
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- Article
Cloning and characterization of the inversion breakpoint at chromosome 2q35 in a patient with Waardenburg syndrome type I.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 5, p. 315
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- Article
Multicolor fluorescence in situ hybridization for the simultaneous detection of probe sets for chromosomes 13, 18, 21, X and Y in uncultured amniotic fluid cells.
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- Human Molecular Genetics, 1992, v. 1, n. 5, p. 307
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Constitutional mutations in the WT1 gene in patients with Denys-Drash syndrome.
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- Human Molecular Genetics, 1992, v. 1, n. 5, p. 301
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The ‘colorizing’ of cytogenetics: is it ready for prime time?
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 5, p. 297
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- Article
Dominant negative mutations in the Wilms tumour (WT1) gene cause Denys-Drash syndrome—proof that a tumour-suppressor gene plays a crucial role in normal genitourinary development.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 5, p. 293
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- Article
Two Taql polymorphisms at the human PGM1 locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 5, p. 354
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- Article
Dinucleotide repeat polymorphism in the human estrogen receptor (ESR) gene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 5, p. 354
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- Article
Dinucleotide repeat polymorphism at the human gene for the brainderived neurotrophic factor (BDNF).
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 5, p. 353
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- Publication type:
- Article
Single base polymorphism in the human Tumour Necrosis Factor alpha (TNFα) gene detectable by Ncol restriction of PCR product.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 5, p. 353
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- Article
Two Mspl polymorphisms within the APC gene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 5, p. 352
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- Article
SAM 1.1 and JOSH 4.4: two RFLPs within the human DCC gene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 5, p. 352
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- Article
Additional polymorphism at a CHR 9 reference locus (D9S12).
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 5, p. 351
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- Article
An Mspl RFLP in the human ARNT gene, encoding a subunit of the nuclear form of the Ah (dioxin) receptor.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 5, p. 351
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- Article
Taql polymorphism at the alanine: glyoxylate aminotransferase (AGXT) gene locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 5, p. 350
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- Article
Dinucleotide repeat polymorphism at the D21S65 locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 5, p. 350
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- Article
A two-allele Pstl RFLP for the alpha-1C adrenergic receptor gene (ADRA1C).
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 5, p. 349
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- Article
Dinucleotide repeat polymorphism at the D4S251 locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 5, p. 349
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- Publication type:
- Article