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Hanan H Afifi

Showing results (1-10 of 37) with videos related to

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Indian Journal of Human Genetics|September 11, 2013
Body composition in Egyptian Turner syndrome girlsMoushira Erfan Zaki, Hanan H Afifi
American Journal of Medical Genetics. Part A|March 18, 2011
Congenital isolated leukonychia totalis in three Egyptian sibsHanan H Afifi, Mahmoud F Abdel-Hamid, Maha S Zaki
American Journal of Medical Genetics. Part A|July 18, 2009
Familial congenital unilateral cerebral ventriculomegaly: Delineation of a distinct genetic disorderMaha S Zaki, Hanan H Afifi, A J Barkovich, et al.
Orphanet Journal of Rare Diseases|January 25, 2014
The supposed tumor suppressor gene WWOX is mutated in an early lethal microcephaly syndrome with epilepsy, growth retardation and retinal degenerationGhada Abdel-Salam, Michaela Thoenes, Hanan H Afifi, et al.
American Journal of Perinatology|February 26, 2021
Genetic Implications in High-Risk Pregnancy and Its Outcome: A 2-Year StudyHanan H Afifi, Khaled R Gaber, Manal M Thomas, et al.
American Journal of Medical Genetics. Part A|July 20, 2012
Growth charts of Down syndrome in Egypt: a study of 434 children 0-36 months of ageHanan H Afifi, Mona S Aglan, Moushira E Zaki, et al.
American Journal of Medical Genetics. Part A|August 1, 2012
Growth curves of Egyptian patients with Turner syndromeHala T El-Bassyouni, Hanan H Afifi, Mona S Aglan, et al.
Neuroradiology|August 4, 2018
Magnetic resonance imaging of developmental facial paresis: a spectrum of complex anomaliesShaimaa Abdelsattar Mohammad, Tougan Taha Abdelaziz, Mohamed I Gadelhak, et al.
Pediatric Dermatology|June 23, 2011
Ectodermal abnormalities in patients with Kabuki syndromeGhada M H Abdel-Salam, Hanan H Afifi, Maha M Eid, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|November 5, 2013
Mutational analysis of the PTPN11 gene in Egyptian patients with Noonan syndromeMona L Essawi, Manal F Ismail, Hanan H Afifi, et al.
Pageof 4

Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
Indian Journal of Human Genetics|September 11, 2013
Body composition in Egyptian Turner syndrome girlsMoushira Erfan Zaki, Hanan H Afifi
American Journal of Medical Genetics. Part A|March 18, 2011
Congenital isolated leukonychia totalis in three Egyptian sibsHanan H Afifi, Mahmoud F Abdel-Hamid, Maha S Zaki
American Journal of Medical Genetics. Part A|July 18, 2009
Familial congenital unilateral cerebral ventriculomegaly: Delineation of a distinct genetic disorderMaha S Zaki, Hanan H Afifi, A J Barkovich, et al.
Orphanet Journal of Rare Diseases|January 25, 2014
The supposed tumor suppressor gene WWOX is mutated in an early lethal microcephaly syndrome with epilepsy, growth retardation and retinal degenerationGhada Abdel-Salam, Michaela Thoenes, Hanan H Afifi, et al.
American Journal of Perinatology|February 26, 2021
Genetic Implications in High-Risk Pregnancy and Its Outcome: A 2-Year StudyHanan H Afifi, Khaled R Gaber, Manal M Thomas, et al.
American Journal of Medical Genetics. Part A|July 20, 2012
Growth charts of Down syndrome in Egypt: a study of 434 children 0-36 months of ageHanan H Afifi, Mona S Aglan, Moushira E Zaki, et al.
American Journal of Medical Genetics. Part A|August 1, 2012
Growth curves of Egyptian patients with Turner syndromeHala T El-Bassyouni, Hanan H Afifi, Mona S Aglan, et al.
Neuroradiology|August 4, 2018
Magnetic resonance imaging of developmental facial paresis: a spectrum of complex anomaliesShaimaa Abdelsattar Mohammad, Tougan Taha Abdelaziz, Mohamed I Gadelhak, et al.
Pediatric Dermatology|June 23, 2011
Ectodermal abnormalities in patients with Kabuki syndromeGhada M H Abdel-Salam, Hanan H Afifi, Maha M Eid, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|November 5, 2013
Mutational analysis of the PTPN11 gene in Egyptian patients with Noonan syndromeMona L Essawi, Manal F Ismail, Hanan H Afifi, et al.
Pageof 4