Works matching IS 03406717 AND DT 2002 AND VI 110 AND IP 6
Results: 11
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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- Article
Homogeneity and distinctiveness of Polish paternal lineages revealed by Y chromosome microsatellite haplotype analysis.
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- Human Genetics, 2002, v. 110, n. 6, p. 592, doi. 10.1007/s00439-002-0728-0
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Distribution of intrachromosomal telomeric sequences (ITS) on Macaca fascicularis (Primates) chromosomes and their implication for chromosome evolution.
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- Human Genetics, 2002, v. 110, n. 6, p. 578, doi. 10.1007/s00439-002-0730-6
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- Article
Presence of fetal DNA in maternal plasma decades after pregnancy.
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- Human Genetics, 2002, v. 110, n. 6, p. 587, doi. 10.1007/s00439-002-0725-3
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- Article
Mutation analysis of the MKKS gene in McKusick-Kaufman syndrome and selected Bardet-Biedl syndrome patients.
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- Human Genetics, 2002, v. 110, n. 6, p. 561, doi. 10.1007/s00439-002-0733-3
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- Article
CYP3A4-V and prostate cancer in African Americans: causal or confounding association because of population stratification?
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- Human Genetics, 2002, v. 110, n. 6, p. 553, doi. 10.1007/s00439-002-0731-5
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- Article
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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- Article
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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- Article
Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC.
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- Human Genetics, 2002, v. 110, n. 6, p. 527, doi. 10.1007/s00439-002-0732-4
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- Article
MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain.
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- Human Genetics, 2002, v. 110, n. 6, p. 545, doi. 10.1007/s00439-002-0724-4
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- Article
PKLR-GBA region shows almost complete linkage disequilibrium over 70 kb in a set of worldwide populations.
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- Human Genetics, 2002, v. 110, n. 6, p. 532, doi. 10.1007/s00439-002-0734-2
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- Article