Works matching IS 14345161 AND DT 2006 AND VI 51 AND IP 1
Results: 12
Linkage analysis of two families with X-linked recessive congenital motor nystagmus.
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- Journal of Human Genetics, 2006, v. 51, n. 1, p. 76, doi. 10.1007/s10038-005-0316-y
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Dent’s disease and prevalence of renal stones in dialysis patients in Northeastern Italy.
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- Journal of Human Genetics, 2006, v. 51, n. 1, p. 25, doi. 10.1007/s10038-005-0317-x
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PAX9 and TGFB3 are linked to susceptibility to nonsyndromic cleft lip with or without cleft palate in the Japanese: population-based and family-based candidate gene analyses.
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- Journal of Human Genetics, 2006, v. 51, n. 1, p. 38, doi. 10.1007/s10038-005-0319-8
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Analysis of the NSD1 promoter region in patients with a Sotos syndrome phenotype.
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- Journal of Human Genetics, 2006, v. 51, n. 1, p. 15, doi. 10.1007/s10038-005-0314-0
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Studies of S-adenosylhomocysteine-hydrolase polymorphism in a Croatian population.
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- Journal of Human Genetics, 2006, v. 51, n. 1, p. 21, doi. 10.1007/s10038-005-0315-z
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Association of CD14 promoter polymorphisms and soluble CD14 levels in mite allergen sensitization of children in Taiwan.
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- Journal of Human Genetics, 2006, v. 51, n. 1, p. 59, doi. 10.1007/s10038-005-0323-z
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Dual origins of the Japanese: common ground for hunter-gatherer and farmer Y chromosomes.
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- Journal of Human Genetics, 2006, v. 51, n. 1, p. 47, doi. 10.1007/s10038-005-0322-0
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Association of alcohol dehydrogenase 2*1 allele with liver damage and insulin concentration in the Japanese.
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- Journal of Human Genetics, 2006, v. 51, n. 1, p. 31, doi. 10.1007/s10038-005-0318-9
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Genetic history of some western Mediterranean human isolates through mtDNA HVR1 polymorphisms.
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- Journal of Human Genetics, 2006, v. 51, n. 1, p. 9, doi. 10.1007/s10038-005-0324-y
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BBS8 is rarely mutated in a cohort of 128 Bardet–Biedl syndrome families.
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- Journal of Human Genetics, 2006, v. 51, n. 1, p. 81, doi. 10.1007/s10038-005-0320-2
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Recent advances in the molecular basis of Lafora’s progressive myoclonus epilepsy.
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- Journal of Human Genetics, 2006, v. 51, n. 1, p. 1, doi. 10.1007/s10038-005-0321-1
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Characterisation of a non-recurrent familial translocation t(7;9)(q11.23;p24.3) points to a recurrent involvement of the Williams–Beuren syndrome region in chromosomal rearrangements.
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- Journal of Human Genetics, 2006, v. 51, n. 1, p. 68, doi. 10.1007/s10038-005-0326-9
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- Article