Works matching IS 14345161 AND DT 1999 AND VI 44 AND IP 1
Results: 18
Repeat-directed isolation of a novel gene preferentially expressed from the maternal allele in human placenta.
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- Journal of Human Genetics, 1999, v. 44, n. 1, p. 1, doi. 10.1007/s100380050096
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Genome-wide scanning for type 2 diabetes susceptibility in Canadian Oji-Cree, using 190 microsatellite markers.
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- Journal of Human Genetics, 1999, v. 44, n. 1, p. 10, doi. 10.1007/s100380050097
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Anxiety traits associated with a polymorphism in the serotonin transporter gene regulatory region in the Japanese.
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- Journal of Human Genetics, 1999, v. 44, n. 1, p. 15, doi. 10.1007/s100380050098
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Germline mutations in a polycytosine repeat of the hMSH6 gene in Korean hereditary nonpolyposis colorectal cancer.
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- Journal of Human Genetics, 1999, v. 44, n. 1, p. 18, doi. 10.1007/s100380050099
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Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese.
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- Journal of Human Genetics, 1999, v. 44, n. 1, p. 22, doi. 10.1007/s100380050100
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Allelic variations of the D2 dopamine receptor gene in children with idiopathic short stature.
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- Journal of Human Genetics, 1999, v. 44, n. 1, p. 26, doi. 10.1007/s100380050101
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Prevalence of congenital malformations and genetic diseases in Korea.
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- Journal of Human Genetics, 1999, v. 44, n. 1, p. 30, doi. 10.1007/s100380050102
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Molecular analysis of methylmalonyl-CoA mutase deficiency: identification of three missense mutations in mut[sup 0] patients.
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- Journal of Human Genetics, 1999, v. 44, n. 1, p. 35, doi. 10.1007/s100380050103
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No latent chromosome damage in oxygen-exposed premature neonates.
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- Journal of Human Genetics, 1999, v. 44, n. 1, p. 40
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Novel germline mutations of the MEN1 gene in Japanese patients with multiple endocrine neoplasia type 1.
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- Journal of Human Genetics, 1999, v. 44, n. 1, p. 43, doi. 10.1007/s100380050105
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Four novel mutations of the Fanconi anemia group A gene (FAA) in Japanese patients.
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- Journal of Human Genetics, 1999, v. 44, n. 1, p. 48, doi. 10.1007/s100380050106
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Molecular cloning, mapping, and characterization of a novel human gene, MTA1-L1, showing homology to a metastasis-associated gene, MTA1.
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- Journal of Human Genetics, 1999, v. 44, n. 1, p. 52, doi. 10.1007/s100380050107
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Localization of human midisatellite and macrosatellite DNA sequences on chromosomes 1 and X in the great apes.
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- Journal of Human Genetics, 1999, v. 44, n. 1, p. 57, doi. 10.1007/s100380050108
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Autosomal dominant onychodystrophy and congenital sensorineural deafness.
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- Journal of Human Genetics, 1999, v. 44, n. 1, p. 60, doi. 10.1007/s100380050109
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Another observation of microphthalmia in an XX male: microphthalmia with linear skin defects syndrome without linear skin lesions.
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- Journal of Human Genetics, 1999, v. 44, n. 1, p. 63, doi. 10.1007/s100380050110
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First case of missense mutation (LDH-H:R171P) in exon 4 of the lactate dehydrogenase gene detected in a Japanese patient.
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- Journal of Human Genetics, 1999, v. 44, n. 1, p. 69, doi. 10.1007/s100380050111
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Chromosomal mapping of two RBP-J-related genes: Kyo-T and RBP-L.
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- Journal of Human Genetics, 1999, v. 44, n. 1, p. 73, doi. 10.1007/s100380050112
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A single-nucleotide polymorphism in the human bone morphogenetic protein-4 (BMP 4) gene.
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- Journal of Human Genetics, 1999, v. 44, n. 1, p. 76, doi. 10.1007/s100380050113
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