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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 stature
S 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 syndrome
S 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 stature
N A Al-Torki, M A Sabry, A Al-Tawari, et al.
Journal of Medical Genetics
|
October 23, 1998
Triophthalmia and facial clefting: a case report
S 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 anomalies
S 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 ectopia
E S Mahfouz, M A Issa, T I Farag, et al.
Page
of 9
Search research articles
Search
Showing results (41-50 of 87) with videos related to
Sort By:
Page
of 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 stature
S 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 syndrome
S 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 stature
N A Al-Torki, M A Sabry, A Al-Tawari, et al.
Journal of Medical Genetics
|
October 23, 1998
Triophthalmia and facial clefting: a case report
S 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 anomalies
S 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 ectopia
E S Mahfouz, M A Issa, T I Farag, et al.
Page
of 9