Commentary: Impact of a deletion of the full-length and short isoform of p75NTR on cholinergic innervation and the population of postmitotic doublecortin positive cells in the dentate gyrus
Sabry, Mohamed A, Fares, Mona, Folkesson, Ronnie, Al-Ramadan, Mariam, Alabkal, Jarrah, Al-Kafaji, Ghada, Hassan, Moustapha
Published in Frontiers in neuroanatomy (19.02.2016)
Published in Frontiers in neuroanatomy (19.02.2016)
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Journal Article
Kenny-Caffey syndrome: an Arab variant?
Sabry, MA, Farag, TI, Shaltout, AA, Zaki, M, Al-Mazidi, Z, Abulhassan, SJ, Al-Torki, N, Quishawi, A, Al Awadi, SA
Published in Clinical genetics (01.01.1999)
Published in Clinical genetics (01.01.1999)
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Journal Article
Total truncation of the molybdopterin/dimerization domains of SUOX protein in an Arab family with isolated sulfite oxidase deficiency
Seidahmed, M.Z., Alyamani, E.A., Rashed, M.S., Saadallah, A.A., Abdelbasit, O.B., Shaheed, M.M., Rasheed, A., Hamid, F.A., Sabry, M.A.
Published in American journal of medical genetics. Part A (15.07.2005)
Published in American journal of medical genetics. Part A (15.07.2005)
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Journal Article
Kenny-Caffey syndrome is part of the CATCH 22 haploinsufficiency cluster
Sabry, M A, Zaki, M, Abul Hassan, S J, Ramadan, D G, Abdel Rasool, M A, al Awadi, S A, al Saleh, Q
Published in Journal of medical genetics (01.01.1998)
Published in Journal of medical genetics (01.01.1998)
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Journal Article
Lissencephaly revisited
Sabry, M A, Farah, S A, Farag, T I
Published in Journal of the American Academy of Child and Adolescent Psychiatry (01.09.1998)
Published in Journal of the American Academy of Child and Adolescent Psychiatry (01.09.1998)
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Journal Article
Triophthalmia and facial clefting: a case report
Tayel, S M, Sabry, M A, Kader, N A, Farah, S, Al-Awadi, S A, Farag, T I
Published in Journal of medical genetics (01.10.1998)
Published in Journal of medical genetics (01.10.1998)
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Journal Article
Right upper limb bub triplication and polythelia, left sided hemihypertrophy and congenital hip dislocation, facial dysmorphism, congenital heart disease, and scoliosis: Disorganisation-like spectrum or patterning gene defect?
Sabry, MA, Al-Saleh, Q, Al-Saw'an, R, Al-Awadi, SA, Farag, TI
Published in Journal of medical genetics (01.01.1995)
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Published in Journal of medical genetics (01.01.1995)
Journal Article
Lissencephaly associated with cerebellar hypoplasia and myoclonic epilepsy in a Bedouin kindred: a new syndrome?
Farah, S., Sabry, M. A., Khuraibet, A., Khaffagi, S., Rudwan, M., Hassan, M., Haseeb, N., Abulhassan, S., Abdel-Rasool, M. A., Elgamal, S., Qasrawi, B., Al-Busairi, W., Farag, T. I.
Published in Clinical genetics (01.05.1997)
Published in Clinical genetics (01.05.1997)
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Journal Article
Genotypic/phenotypic heterogeneity of selective vitamin B12 malabsorption (Grasbeck-Imerslund syndrome) in two Bedouin families
Ismail, EAR, Saleh, Q Al, Sabry, MA, Ghanim, M Al, Zaki, M
Published in Acta Paediatrica (01.04.1997)
Published in Acta Paediatrica (01.04.1997)
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Journal Article
Unusual traits associated with Robinow syndrome
Sabry, M A, Ismail, E A, al-Naggar, R L, al-Torki, N A, Farah, S, al-Awadi, S A, Obenbergerova, D, Bastaki, L
Published in Journal of medical genetics (01.09.1997)
Published in Journal of medical genetics (01.09.1997)
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