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S A Al-Awadi

Showing results (41-50 of 87) with videos related to

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Journal of Medical Genetics|October 1, 1987
A family with spondyloepimetaphyseal dwarfism: a 'new' dysplasia or Kniest disease with autosomal recessive inheritance?T I Farag, S A Al-Awadi, M C Hunt, et al.
Annales De Genetique|January 1, 1990
Mosaicism 45,X/46,X, t dic(Xp:Xp) in a girl with short statureS J Abulhasan, A S Teebi, M Zaki, et al.
Journal of Medical Genetics|June 3, 1999
Familial pericentric inversion of chromosome 1 (p36.3q23) and Bardet-Biedl syndromeS M Tayel, R L Al-Naggar, D S Krishna Murthy, et al.
American Journal of Medical Genetics|September 17, 1998
Craniofacial dyssynostosis with cryptorchidism and normal statureN A Al-Torki, M A Sabry, A Al-Tawari, et al.
Journal of Medical Genetics|October 23, 1998
Triophthalmia and facial clefting: a case reportS M Tayel, M A Sabry, N A Kader, et al.
The British Journal of Psychiatry : the Journal of Mental Science|December 1, 1989
Familial manic-depressive illness with deleted short arm of chromosome 21: coincidental or causal?M H el-Badramany, T I Farag, S A al-Awadi, et al.
Journal of Medical Genetics|December 1, 1983
Interstitial deletion of the long arm of chromosome 2: del(2)(q31q33)S A Al-Awadi, T I Farag, K Naguib, et al.
Annals of Saudi Medicine|February 7, 2007
Clustering of trisomy 18 in Kuwait: Genetic predisposition or environmental?K K Naguib, S A Al-Awadi, L Bastaki, et al.
Annals of Saudi Medicine|August 27, 2005
A morpho-etiological description of congenital limb anomaliesS M Tayel, M M Fawzia, Niran A Al-Naqeeb, et al.
Journal of Pediatric Surgery|June 1, 1990
Persistent Mullerian duct syndrome: report of two boys with associated crossed testicular ectopiaE S Mahfouz, M A Issa, T I Farag, et al.
Pageof 9

Showing results (41-50 of 87) with videos related to

Sort By:
Pageof 9
Journal of Medical Genetics|October 1, 1987
A family with spondyloepimetaphyseal dwarfism: a 'new' dysplasia or Kniest disease with autosomal recessive inheritance?T I Farag, S A Al-Awadi, M C Hunt, et al.
Annales De Genetique|January 1, 1990
Mosaicism 45,X/46,X, t dic(Xp:Xp) in a girl with short statureS J Abulhasan, A S Teebi, M Zaki, et al.
Journal of Medical Genetics|June 3, 1999
Familial pericentric inversion of chromosome 1 (p36.3q23) and Bardet-Biedl syndromeS M Tayel, R L Al-Naggar, D S Krishna Murthy, et al.
American Journal of Medical Genetics|September 17, 1998
Craniofacial dyssynostosis with cryptorchidism and normal statureN A Al-Torki, M A Sabry, A Al-Tawari, et al.
Journal of Medical Genetics|October 23, 1998
Triophthalmia and facial clefting: a case reportS M Tayel, M A Sabry, N A Kader, et al.
The British Journal of Psychiatry : the Journal of Mental Science|December 1, 1989
Familial manic-depressive illness with deleted short arm of chromosome 21: coincidental or causal?M H el-Badramany, T I Farag, S A al-Awadi, et al.
Journal of Medical Genetics|December 1, 1983
Interstitial deletion of the long arm of chromosome 2: del(2)(q31q33)S A Al-Awadi, T I Farag, K Naguib, et al.
Annals of Saudi Medicine|February 7, 2007
Clustering of trisomy 18 in Kuwait: Genetic predisposition or environmental?K K Naguib, S A Al-Awadi, L Bastaki, et al.
Annals of Saudi Medicine|August 27, 2005
A morpho-etiological description of congenital limb anomaliesS M Tayel, M M Fawzia, Niran A Al-Naqeeb, et al.
Journal of Pediatric Surgery|June 1, 1990
Persistent Mullerian duct syndrome: report of two boys with associated crossed testicular ectopiaE S Mahfouz, M A Issa, T I Farag, et al.
Pageof 9