Dinucleotide repeat polymorphism at the human erythroid alpha spectrin (SPTA1) locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 218
- By:
- Publication type:
- Article
Works matching IS 09646906 AND DT 1992 AND VI 1 AND IP 3
Results: 28
1
2
Dinucleotide repeat polymorphism at the HOX 2B locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 218
- By:
- Publication type:
- Article
3
An Alu variable polyA repeat polymorphism upstream of L-myc at 1p32.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 217
- By:
- Publication type:
- Article
4
An STS from a cDNA located in the myotonic dystrophy region (DM) on human chromosome 19q13.3.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 217
- By:
- Publication type:
- Article
5
Dinucleotide repeat polymorphism in the human fibroblast growth factor acidic (FGFA) gene on chromosome 5.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 216
- By:
- Publication type:
- Article
6
Dinucleotide repeat polymorphism at the DXS178 locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 216
- By:
- Publication type:
- Article
7
The PAX3 gene is mapped to human chromosome 2 together with a highly informative CA dinucleotide repeat.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 215
- By:
- Publication type:
- Article
8
Dinucleotide repeat polymorphism in the Huntington's disease region at the D4S43 locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 215
- By:
- Publication type:
- Article
9
Author index.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 219
- Publication type:
- Article
10
Microsatellite polymorphisms at the D11S554 and D11S569 loci.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 214
- By:
- Publication type:
- Article
11
Dinucleotide repeat polymorphisms at the DXS365, DXS443 and DXS451 loci.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 213
- By:
- Publication type:
- Article
12
Standards for reporting alleles at highly polymorphic loci: a proposal.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 211
- By:
- Publication type:
- Article
13
G6PD Kalyan and G6PD Kerala; two deficient variants in India caused by the same 317 Glu↑Lys mutation.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 209
- By:
- Publication type:
- Article
14
A novel mutation in the p53 gene in a Burkitt's lymphoma cell line.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 207
- By:
- Publication type:
- Article
15
A novel C to T substitution at nucleotide 1360 of cDNA which abolishes a natural Hha l site accounts for a new G6PD deficiency gene in Chinese.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 205
- By:
- Publication type:
- Article
16
Transcription of deleted mitochondrial DNA in human colon adenocarcinoma cells.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 203
- By:
- Publication type:
- Article
17
cA479 (D3S719): a cosmid mapped telomeric of the Von Hippel Lindau disease gene contains the D3S18 locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 201
- By:
- Publication type:
- Article
18
Sequence of the exon-containing regions of the human factor VIII gene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 199
- By:
- Publication type:
- Article
19
Molecular analysis of patients with Hunter syndrome: implication of a region prone to structural alterations within the IDS gene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 195
- By:
- Publication type:
- Article
20
An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5′ end of the monoamine oxidase A gene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 187
- By:
- Publication type:
- Article
21
Isolation and sequence of two genes associated with a CpG island 5′ of the factor VIII gene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 179
- By:
- Publication type:
- Article
22
Genetic linkage of the human gene for phenylethanol-amine N-methyltransferase (PNMT), the adrenaline-synthesizing enzyme, to DNA markers on chromosome 17q21–q22.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 175
- By:
- Publication type:
- Article
23
Both mutations in G6PD A — are necessary to produce the G6PD deficient phenotype.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 171
- By:
- Publication type:
- Article
24
The search for Y chromosome polymorphism is extended to negroids.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 169
- By:
- Publication type:
- Article
25
Characterization of a YAC containing part or all of the Norrie disease locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 161
- By:
- Publication type:
- Article
26
Cloning of the Huntington disease region in yeast artificial chromosomes.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 149
- By:
- Publication type:
- Article
27
ACE (or PNMT?) in the hole.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 147
- By:
- Publication type:
- Article
28
Screening for mutations in the open reading frame and promoter of the β-amyloid precursor protein gene in familial Alzheimer's disease: identification of a further family with APP717 Val→lle.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 165
- By:
- Publication type:
- Article