Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Mohammed Tolefat"'
Autor:
Fouad Alshaban, Mohammed Aldosari, Zakaria El Sayed, Mohammed Tolefat, Saba El Hag, Hawra Al Shammari, Iman Ghazal, Eric Fombonne
Publikováno v:
Autism and Developmental Language Impairments, Vol 2 (2017)
Autism spectrum disorder (ASD) is an increasingly prevalent disorder. Although around 15% of cases are caused by specific genetic causes, most cases involve a complex and variable combination of genetic risk and environmental factors that are not yet
Externí odkaz:
https://doaj.org/article/960c6d38cdf84bb499fe27e453307ac0
Autor:
Yasser Al-Sarraj BSC, Tawfeg Ben-Omran MD, Mohammed Tolefat MBBS, Yosra Bejaoui MSc, Hatem El-Shanti MD, Marios Kambouris PhD
Publikováno v:
Journal of Inborn Errors of Metabolism and Screening, Vol 2 (2014)
A consanguineous Qatari family having an autosomal recessive disorder characterized by severe mental retardation, cerebellar vermis hypoplasia, retinal degeneration, optic nerve atrophy, ataxic gait, and seizures was studied for identification of the
Externí odkaz:
https://doaj.org/article/2892747a39bc456f9bce7d7112296d43
Autor:
Zakaria El Sayed, Hawra Al Shammari, Saba El Hag, Iman Ghazal, Eric Fombonne, Fouad Alshaban, Mohammed Aldosari, Mohammed Tolefat
Publikováno v:
Autism & Developmental Language Impairments, Vol 2 (2017)
Autism spectrum disorder (ASD) is an increasingly prevalent disorder. Although around 15% of cases are caused by specific genetic causes, most cases involve a complex and variable combination of genetic risk and environmental factors that are not yet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::744ce1afe72e2e2b319cd6256d715da1
https://doaj.org/article/960c6d38cdf84bb499fe27e453307ac0
https://doaj.org/article/960c6d38cdf84bb499fe27e453307ac0
Publikováno v:
Qatar Foundation Annual Research Forum Volume 2012 Issue 1.
A consanguineous Qatari family affected by a novel autosomal recessive disorder characterized by severe mental retardation, retinal degeneration, optic nerve atrophy, ataxic gait and edematous puffiness of hands was studied by genome-wide SNP genotyp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cada79f032a54ce0bc472e714f166439
https://doi.org/10.5339/qfarf.2012.bmp100
https://doi.org/10.5339/qfarf.2012.bmp100
Autor:
Hatem El-Shanti, Marios Kambouris, Mohammed Tolefat, Yasser Al-Sarraj, Tawfeg Ben-Omran, Yosra Bejaoui
Publikováno v:
Journal of Inborn Errors of Metabolism and Screening. 2:232640981455052
A consanguineous Qatari family having an autosomal recessive disorder characterized by severe mental retardation, cerebellar vermis hypoplasia, retinal degeneration, optic nerve atrophy, ataxic gait, and seizures was studied for identification of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a5f3728ae7c455f5ae28465677debbc
https://doi.org/10.1177/2326409814550528
https://doi.org/10.1177/2326409814550528