Výsledky vyhledávání - "Ghing Billedo"

Discovery of a Probable Gene Mutation Causing Mental Retardation, Microsomia, and Signs of Skeletal Dysplasia in an Arab Family with a Previously Undelineated Autosomal Recessive Disorder

Autor: Mazen Osman, Jamil Alami, Hatem El-Shanti, Ghing Billedo, Yasser Al-Sarraj, Samiha Zaineddin

Publikováno v: Qatar Foundation Annual Research Forum Proceedings. :BMP62

Background: Autosomal recessive diseases are considered as a major group of single-gene disorders among Arab population. We have recruited a family with three siblings with a mental retardation (MR) syndrome who were born to consanguineous Qatari par

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::23d4c7d8c808f609ea435b4aeb5075ff
https://doi.org/10.5339/qfarf.2011.bmp62

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