CYP3A4-V and prostate cancer in African Americans: causal or confounding association because of population stratification?
- Published in:
- Human Genetics, 2002, v. 110, n. 6, p. 553, doi. 10.1007/s00439-002-0731-5
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- Publication type:
- Article
Works matching IS 03406717 AND DT 2002 AND VI 110 AND IP 6
Results: 11
1
2
PKLR-GBA region shows almost complete linkage disequilibrium over 70 kb in a set of worldwide populations.
- Published in:
- Human Genetics, 2002, v. 110, n. 6, p. 532, doi. 10.1007/s00439-002-0734-2
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- Publication type:
- Article
3
Allelic and locus heterogeneity in autosomal recessive gelatinous drop-like corneal dystrophy.
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- Human Genetics, 2002, v. 110, n. 6, p. 568, doi. 10.1007/s00439-002-0729-z
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- Publication type:
- Article
4
Homogeneity and distinctiveness of Polish paternal lineages revealed by Y chromosome microsatellite haplotype analysis.
- Published in:
- Human Genetics, 2002, v. 110, n. 6, p. 592, doi. 10.1007/s00439-002-0728-0
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- Publication type:
- Article
5
Distribution of intrachromosomal telomeric sequences (ITS) on Macaca fascicularis (Primates) chromosomes and their implication for chromosome evolution.
- Published in:
- Human Genetics, 2002, v. 110, n. 6, p. 578, doi. 10.1007/s00439-002-0730-6
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- Publication type:
- Article
6
Presence of fetal DNA in maternal plasma decades after pregnancy.
- Published in:
- Human Genetics, 2002, v. 110, n. 6, p. 587, doi. 10.1007/s00439-002-0725-3
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- Publication type:
- Article
7
Mutation analysis of the MKKS gene in McKusick-Kaufman syndrome and selected Bardet-Biedl syndrome patients.
- Published in:
- Human Genetics, 2002, v. 110, n. 6, p. 561, doi. 10.1007/s00439-002-0733-3
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- Publication type:
- Article
8
MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain.
- Published in:
- Human Genetics, 2002, v. 110, n. 6, p. 545, doi. 10.1007/s00439-002-0724-4
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- Publication type:
- Article
9
Timing of the absence of FMR1 expression in full mutation chorionic villi.
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- Human Genetics, 2002, v. 110, n. 6, p. 601, doi. 10.1007/s00439-002-0723-5
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- Publication type:
- Article
10
Allele-specific PCR amplification due to sequence identity between a PCR primer and an amplicon : is direct sequencing so reliable?
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- Human Genetics, 2002, v. 110, n. 6, p. 606, doi. 10.1007/s00439-002-0735-1
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- Publication type:
- Article
11
Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC.
- Published in:
- Human Genetics, 2002, v. 110, n. 6, p. 527, doi. 10.1007/s00439-002-0732-4
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- Publication type:
- Article