학술논문
Diagnostic Exome Sequencing to Elucidate the Genetic Basis of Likely Recessive Disorders in Consanguineous Families
Document Type
Article
Author
Makrythanasis, P.; Nelis, M.; Santoni, F.A.; Vannier, A.; Bustamante Eduardo, M.; Stamoulis, G.; Hamamy, H.; Antonarakis, S.E.; Guipponi, M.; Béna, F.; Gimelli, S.; Stathaki, E.; Bottani, A.; Fokstuen, S.; Gwanmesia, L.; Aliferis, K.; Temtamy, S.; Aglan, M.S.; Zaki, M.S.; Mégarbané, A.; Jalkh, N.; Masri, A.; Psoni, S.; Kitsiou-Tzeli, S.; Fryssira, H.; Kanavakis, E.; Al-Allawi, N.; Sefiani, A.; Elalaoui, S.C.; Al Hait, S.; Al-Gazali, L.; Al-Jasmi, F.; Bouhamed, H.C.; Abdalla, E.; Cooper, D.N.
Source
In: Human Mutation . (Human Mutation, 1 October 2014, 35(10):1203-1210)
Subject
Language
English
ISSN
10981004
10597794
10597794