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M A Sabry

Showing results (21-30 of 33) with videos related to

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Journal of Medical Genetics|October 23, 1998
Triophthalmia and facial clefting: a case reportS M Tayel, M A Sabry, N A Kader, et al.
American Journal of Medical Genetics|January 10, 1997
Another Arab patient with overlap of Váradi-Papp/Opitz trigonocephaly syndromes?M A Sabry, Q al Saleh, S Farah, et al.
Journal of Medical Genetics|February 1, 1996
Femoral hypoplasia-unusual facies syndrome with bifid hallux, absent tibia, and macrophallus: a report of a Bedouin babyM A Sabry, D Obenbergerova, R Al-Sawan, et al.
Clinical Neurology and Neurosurgery|February 1, 1997
Hereditary spastic paraparesis with distal muscle wasting, microcephaly, mental retardation, arachnodactyly and tremors: new entity?S Farah, M A Sabry, A F al-Shubaili, et al.
Journal of Medical Genetics|February 25, 1998
Kenny-Caffey syndrome is part of the CATCH 22 haploinsufficiency clusterM A Sabry, M Zaki, S J Abul Hassan, et al.
Journal of Medical Genetics|October 10, 1997
Unusual traits associated with Robinow syndromeM A Sabry, E A Ismail, R L al-Naggar, et al.
Clinical Dysmorphology|May 18, 1999
New syndromic entity of situs inversus totalisM A Mubashir, M A Sabry, S Farah, et al.
Annales De Genetique|January 1, 1996
De novo direct duplication 7p (p11.2-->pter) in an Arab child with MCA/MR syndrome: trisomy 7p a delineated syndrome?M A Redha, D S Krishna Murthy, S A al-Awadi, et al.
Clinical Dysmorphology|May 8, 1998
Cutis verticis gyrata-mental deficiency syndrome: report of a case with unusual neuroradiological findingsS Farah, T Farag, M A Sabry, et al.
American Journal of Medical Genetics. Part A|June 14, 2005
Total truncation of the molybdopterin/dimerization domains of SUOX protein in an Arab family with isolated sulfite oxidase deficiencyM Z Seidahmed, E A Alyamani, M S Rashed, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Journal of Medical Genetics|October 23, 1998
Triophthalmia and facial clefting: a case reportS M Tayel, M A Sabry, N A Kader, et al.
American Journal of Medical Genetics|January 10, 1997
Another Arab patient with overlap of Váradi-Papp/Opitz trigonocephaly syndromes?M A Sabry, Q al Saleh, S Farah, et al.
Journal of Medical Genetics|February 1, 1996
Femoral hypoplasia-unusual facies syndrome with bifid hallux, absent tibia, and macrophallus: a report of a Bedouin babyM A Sabry, D Obenbergerova, R Al-Sawan, et al.
Clinical Neurology and Neurosurgery|February 1, 1997
Hereditary spastic paraparesis with distal muscle wasting, microcephaly, mental retardation, arachnodactyly and tremors: new entity?S Farah, M A Sabry, A F al-Shubaili, et al.
Journal of Medical Genetics|February 25, 1998
Kenny-Caffey syndrome is part of the CATCH 22 haploinsufficiency clusterM A Sabry, M Zaki, S J Abul Hassan, et al.
Journal of Medical Genetics|October 10, 1997
Unusual traits associated with Robinow syndromeM A Sabry, E A Ismail, R L al-Naggar, et al.
Clinical Dysmorphology|May 18, 1999
New syndromic entity of situs inversus totalisM A Mubashir, M A Sabry, S Farah, et al.
Annales De Genetique|January 1, 1996
De novo direct duplication 7p (p11.2-->pter) in an Arab child with MCA/MR syndrome: trisomy 7p a delineated syndrome?M A Redha, D S Krishna Murthy, S A al-Awadi, et al.
Clinical Dysmorphology|May 8, 1998
Cutis verticis gyrata-mental deficiency syndrome: report of a case with unusual neuroradiological findingsS Farah, T Farag, M A Sabry, et al.
American Journal of Medical Genetics. Part A|June 14, 2005
Total truncation of the molybdopterin/dimerization domains of SUOX protein in an Arab family with isolated sulfite oxidase deficiencyM Z Seidahmed, E A Alyamani, M S Rashed, et al.
Pageof 4