Works matching IS 14345161 AND DT 2015 AND VI 60 AND IP 1
Results: 7
Investigation of genetic factors underlying typical orofacial clefts: mutational screening and copy number variation.
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- Journal of Human Genetics, 2015, v. 60, n. 1, p. 17, doi. 10.1038/jhg.2014.96
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- Article
Sousse: extreme genetic heterogeneity in North Africa.
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- Journal of Human Genetics, 2015, v. 60, n. 1, p. 41, doi. 10.1038/jhg.2014.99
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- Article
The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey.
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- Journal of Human Genetics, 2015, v. 60, n. 1, p. 51, doi. 10.1038/jhg.2014.101
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- Article
Association of neonatal hyperbilirubinemia in breast-fed infants with UGT1A1 or SLCOs polymorphisms.
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- Journal of Human Genetics, 2015, v. 60, n. 1, p. 35, doi. 10.1038/jhg.2014.98
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- Article
The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey.
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- Journal of Human Genetics, 2015, v. 60, n. 1, p. 1, doi. 10.1038/jhg.2014.85
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- Article
Genetic variant in NDUFS1 gene is associated with schizophrenia and negative symptoms in Han Chinese.
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- Journal of Human Genetics, 2015, v. 60, n. 1, p. 11, doi. 10.1038/jhg.2014.94
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- Article
Identification of two novel mutations in the NOG gene associated with congenital stapes ankylosis and symphalangism.
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- Journal of Human Genetics, 2015, v. 60, n. 1, p. 27, doi. 10.1038/jhg.2014.97
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- Article