Works matching IS 10184813 AND DT 2002 AND VI 10 AND IP 4
Results: 11
Three novel human VMD2-like genes are members of the evolutionary highly conserved RFP-TM family.
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- European Journal of Human Genetics, 2002, v. 10, n. 4, p. 281, doi. 10.1038/sj.ejhg.5200796
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European combined analysis of the CTG18.1 and the ERDA1 CAG/CTG repeats in bipolar disorder.
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- European Journal of Human Genetics, 2002, v. 10, n. 4, p. 276, doi. 10.1038/sj.ejhg.5200803
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- Article
Sharing of a conserved haplotype suggests a susceptibility gene for multiple sclerosis at chromosome 17p11.
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- European Journal of Human Genetics, 2002, v. 10, n. 4, p. 271, doi. 10.1038/sj.ejhg.5200802
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- Article
Positive association to lgE levels and a physical map of the 13q14 atopy locus.
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- European Journal of Human Genetics, 2002, v. 10, n. 4, p. 266, doi. 10.1038/sj.ejhg.5200801
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Sex stratification of an inflammatory bowel disease genome search shows male-specific linkage to the HLA region of chromosome 6.
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- European Journal of Human Genetics, 2002, v. 10, n. 4, p. 259, doi. 10.1038/sj.ejhg.5200792
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- Article
Fine mapping of the locus for Shwachman-Diamond syndrome at 7q11, identification of shared disease haplotypes, and exclusion of TPST1 as a candidate gene.
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- European Journal of Human Genetics, 2002, v. 10, n. 4, p. 250, doi. 10.1038/sj.ejhg.5200798
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Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa.
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- European Journal of Human Genetics, 2002, v. 10, n. 4, p. 245, doi. 10.1038/sj.ejhg.5200797
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- Article
Analysis of alterations of WFDC1, a new putative tumor suppressor gene, in hepatocellular carcinoma.
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- European Journal of Human Genetics, 2002, v. 10, n. 4, p. 239, doi. 10.1038/sj.ejhg.5200795
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- Article
Multiplex PCR combining deltaF508 mutation and intragenic microsatellites of the CFTR gene for pre-implantation genetic diagnosis (PGD) of cystic fibrosis.
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- European Journal of Human Genetics, 2002, v. 10, n. 4, p. 230
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- Article
MEHMO (Mental retardation, Epileptic seizures, Hypogenitalism, Microcephaly, Obesity): a new X-linked mitochondrial disorder.
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- European Journal of Human Genetics, 2002, v. 10, n. 4, p. 226, doi. 10.1038/sj.ejhg.5200791
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Alpha-thalassemia/mental retardation syndrome, X-Linked (ATR-X, MIM #301040, ATR-X/XNP/XH2 gene MIM #30032.
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- European Journal of Human Genetics, 2002, v. 10, n. 4, p. 223, doi. 10.1038/sj.ejhg.5200800
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- Article