Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Kaoutar Ben Makhlouf"'
Autor:
Yousra Benmakhlouf, Renaud Touraine, Ines Harzallah, Zeineb Zian, Kaoutar Ben Makhlouf, Amina Barakat, Naima Ghailani Nourouti, Mohcine Bennani Mechita
Publikováno v:
BMC Research Notes, Vol 14, Iss 1, Pp 1-5 (2021)
Abstract Objective Intellectual Disability (ID) represents a neuropsychiatric disorder, which its etiopathogenesis remains insufficiently understood. Mutations in the Aristaless Related Homeobox gene (ARX) have been identified to cause syndromic and
Externí odkaz:
https://doaj.org/article/0ca085e180954c6082b8abcd2187fb98
Autor:
Yousra, Benmakhlouf, Zeineb, Zian, Kaoutar, Ben Makhlouf, Naima, Ghailani Nourouti, Amina, Barakat, Mohcine, Bennani Mechita
Publikováno v:
Innov Clin Neurosci
Objective: Intellectual disability (ID) is a heterogeneous group of disorders characterized by a congenital limitation in intellectual functioning and adaptive behaviour. Our present work aimed to describe the demographic and clinical characteristics
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c08c68f284260740e54f7d23e15379de
https://pubmed.ncbi.nlm.nih.gov/33898095
https://pubmed.ncbi.nlm.nih.gov/33898095
Autor:
Zeineb Zian, Renaud Touraine, Naima Ghailani Nourouti, Amina Barakat, Kaoutar Ben Makhlouf, Ines Harzallah, Mohcine Bennani Mechita, Yousra Benmakhlouf
Publikováno v:
BMC Research Notes
BMC Research Notes, Vol 14, Iss 1, Pp 1-5 (2021)
BMC Research Notes, Vol 14, Iss 1, Pp 1-5 (2021)
Objective Intellectual Disability (ID) represents a neuropsychiatric disorder, which its etiopathogenesis remains insufficiently understood. Mutations in the Aristaless Related Homeobox gene (ARX) have been identified to cause syndromic and nonsyndro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26b1dac1126edc36d5492d99e0485816
https://pubmed.ncbi.nlm.nih.gov/33757564
https://pubmed.ncbi.nlm.nih.gov/33757564