Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Samiha, Zaineddin"'
Autor:
Almuriekhi, Mariam, Shintani, Takafumi, Fahiminiya, Somayyeh, Fujikawa, Akihiro, Kuboyama, Kazuya, Takeuchi, Yasushi, Nawaz, Zafar, Nadaf, Javad, Kamel, Hussein, Kitam, Abu Khadija, Samiha, Zaineddin, Mahmoud, Laila, Ben-Omran, Tawfeg, Majewski, Jacek, Noda, Masaharu
Publikováno v:
In Cell Reports 10 March 2015 10(9):1585-1598
Autor:
Vincent Tropepe, Natalie Sorfazlian, Zafar Nawaz, Tawfeg Ben-Omran, Kitam Abu Khadija, Samiha Zaineddin, Mariam Almuriekhi, Hussein Kamel, Jacek Majewski, Somayyeh Fahiminiya, Javad Nadaf
Publikováno v:
Journal of Medical Genetics. 52:381-390
Background Neuroanatomical defects are often present in children with severe developmental delay and intellectual disabilities. Few genetic loci have been associated with disorders of neurodevelopment. Our objective of the present study was to analys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b7d74ee013973aaacccc34549b06627
https://doi.org/10.1136/jmedgenet-2014-102707
https://doi.org/10.1136/jmedgenet-2014-102707
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
https://doi.org/10.5339/qfarf.2011.bmp62
Autor:
Almuriekhi, Mariam, Shintani, Takafumi, Fahiminiya, Somayyeh, Fujikawa, Akihiro, Kuboyama, Kazuya, Takeuchi, Yasushi, Nawaz, Zafar, Nadaf, Javad, Kamel, Hussein, Kitam, Abu Khadija, Samiha, Zaineddin, Mahmoud, Laila, Ben-Omran, Tawfeg, Majewski, Jacek, Noda, Masaharu
Publikováno v:
Cell Reports; March 2015, Vol. 10 Issue: 9 p1585-1598, 14p