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Skin-Dominant Phenotype in a Patient with H Syndrome: Identification of a Novel Mutation in the SLC29A3 Gene.
Vural, Seçil; Ertop, Pelin; Durmaz, Ceren D; Sanli, Hatice; Okçu Heper, Aylin; Kundakçi, Nihal; Karabulut, Halil G; Ilgin Ruhi, Hatice.
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  • Vural S; Department of Dermatology, Faculty of Medicine, Ankara University, Ankara, Turkey.
Cytogenet Genome Res ; 151(4): 186-190, 2017.
Article in En | MEDLINE | ID: mdl-28554179
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin / Skin Diseases / Nucleoside Transport Proteins / Mutation Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Female / Humans Language: En Journal: Cytogenet Genome Res Journal subject: GENETICA Year: 2017 Document type: Article Affiliation country:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin / Skin Diseases / Nucleoside Transport Proteins / Mutation Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Female / Humans Language: En Journal: Cytogenet Genome Res Journal subject: GENETICA Year: 2017 Document type: Article Affiliation country: