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Journal of Medical Genetics
|
February 1, 1991
Human homologue for the mouse mutant disorganisation: does it exist?
K K Naguib, M S Hamoud, E S Khalil, et al.
Journal of the Royal Society of Medicine
|
October 1, 1985
Fibrodysplasia ossificans progressiva
S A Al-Awadi, T I Farag, M Y el-Khalifa, et al.
American Journal of Medical Genetics
|
December 1, 1989
Urofacial syndrome
A S Teebi, T I Farag, M Y el-Khalifa, et al.
European Journal of Pediatrics
|
January 1, 1987
Phenylketonuria in Kuwait and Arab countries
A S Teebi, S A Al-Awadi, T I Farag, et al.
Lancet (London, England)
|
September 22, 1984
Anencephaly: disappearing in Kuwait?
S A Al-Awadi, T I Farag, A S Teebi, et al.
Journal of Medical Genetics
|
February 1, 1985
Profound limb deficiency, thoracic dystrophy, unusual facies, and normal intelligence: a new syndrome
S A Al-Awadi, A S Teebi, T I Farag, et al.
American Journal of Medical Genetics
|
April 1, 1986
Interstitial deletion of the long arm of chromosome 1 [del(1)(q32q42)]
S A Al-Awadi, T I Farag, R Usha, et al.
Clinical Genetics
|
May 1, 1986
The effect of consanguineous marriages on reproductive wastage
S A Al-Awadi, K K Naguib, M A Moussa, et al.
American Journal of Medical Genetics
|
June 1, 1989
Familial uterine hernia syndrome: report of an Arab family with four affected males
K K Naguib, A S Teebi, T I Farag, et al.
Journal of Medical Genetics
|
June 1, 1984
Spondyloepiphyseal dysplasia tarda with progressive arthropathy
S A Al-Awadi, T I Fårag, K Naguib, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Journal of Medical Genetics
|
February 1, 1991
Human homologue for the mouse mutant disorganisation: does it exist?
K K Naguib, M S Hamoud, E S Khalil, et al.
Journal of the Royal Society of Medicine
|
October 1, 1985
Fibrodysplasia ossificans progressiva
S A Al-Awadi, T I Farag, M Y el-Khalifa, et al.
American Journal of Medical Genetics
|
December 1, 1989
Urofacial syndrome
A S Teebi, T I Farag, M Y el-Khalifa, et al.
European Journal of Pediatrics
|
January 1, 1987
Phenylketonuria in Kuwait and Arab countries
A S Teebi, S A Al-Awadi, T I Farag, et al.
Lancet (London, England)
|
September 22, 1984
Anencephaly: disappearing in Kuwait?
S A Al-Awadi, T I Farag, A S Teebi, et al.
Journal of Medical Genetics
|
February 1, 1985
Profound limb deficiency, thoracic dystrophy, unusual facies, and normal intelligence: a new syndrome
S A Al-Awadi, A S Teebi, T I Farag, et al.
American Journal of Medical Genetics
|
April 1, 1986
Interstitial deletion of the long arm of chromosome 1 [del(1)(q32q42)]
S A Al-Awadi, T I Farag, R Usha, et al.
Clinical Genetics
|
May 1, 1986
The effect of consanguineous marriages on reproductive wastage
S A Al-Awadi, K K Naguib, M A Moussa, et al.
American Journal of Medical Genetics
|
June 1, 1989
Familial uterine hernia syndrome: report of an Arab family with four affected males
K K Naguib, A S Teebi, T I Farag, et al.
Journal of Medical Genetics
|
June 1, 1984
Spondyloepiphyseal dysplasia tarda with progressive arthropathy
S A Al-Awadi, T I Fårag, K Naguib, et al.
Page
of 2