Works matching IS 10184813 AND DT 2002 AND VI 10 AND IP 8
Results: 9
A novel polymorphism in exon 11 of the WKL1 gene, shows no association with schizophrenia.
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- European Journal of Human Genetics, 2002, v. 10, n. 8, p. 491, doi. 10.1038/sj.ejhg.5200837
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Mutations of Cx25 gene (GJB2) for prelingual deafness in Taiwan.
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- European Journal of Human Genetics, 2002, v. 10, n. 8, p. 495, doi. 10.1038/sj.ejhg.5200838
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- Article
Low frequency of MECP2 mutations in mentally retarded males.
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- European Journal of Human Genetics, 2002, v. 10, n. 8, p. 487, doi. 10.1038/sj.ejhg.5200836
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- Article
MECP2 gene mutation analysis in Chinese patients with Rett syndrome.
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- European Journal of Human Genetics, 2002, v. 10, n. 8, p. 484, doi. 10.1038/sj.ejhg.5200827
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Both common and unique susceptibility genes in different rat strains with pristane-induced arthritis.
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- European Journal of Human Genetics, 2002, v. 10, n. 8, p. 475
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- Article
Unique (Y;13) translocation in a male with oligozoospermia: cytogenetic and molecular studies.
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- European Journal of Human Genetics, 2002, v. 10, n. 8, p. 467, doi. 10.1038/sj.ejhg.5200835
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- Article
Rapid detection of common autosomal aneuploidies by quantitative fluorescent PCR on uncultured amniocytes.
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- European Journal of Human Genetics, 2002, v. 10, n. 8, p. 462, doi. 10.1038/sj.ejhg.5200833
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Identification of novel SDHD mutations in patients with phaeochromocytoma and/or paraganglioma.
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- European Journal of Human Genetics, 2002, v. 10, n. 8, p. 457, doi. 10.1038/sj.ejhg.5200829
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Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina.
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- European Journal of Human Genetics, 2002, v. 10, n. 8, p. 449, doi. 10.1038/sj.ejhg.5200828
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- Article