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journal of human genetics
سال:2015 - دوره:60 - شماره:1
Association of neonatal hyperbilirubinemia in breast-fed infants with UGT1A1 or SLCOs polymorphisms
- صفحه:35-40
Erratum: The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey
- صفحه:51-51
Genetic variant in NDUFS1 gene is associated with schizophrenia and negative symptoms in Han Chinese
- صفحه:11-16
Identification of two novel mutations in the NOG gene associated with congenital stapes ankylosis and symphalangism
- صفحه:27-34
Investigation of genetic factors underlying typical orofacial clefts: mutational screening and copy number variation
- صفحه:17-25
Sousse: extreme genetic heterogeneity in North Africa
- صفحه:41-49
The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey
- صفحه:1-9
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