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S A Al-Awadi

Showing results (61-70 of 87) with videos related to

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American Journal of Medical Genetics|June 1, 1989
Familial uterine hernia syndrome: report of an Arab family with four affected malesK K Naguib, A S Teebi, T I Farag, et al.
Annals of Saudi Medicine|May 1, 1994
Mixed gonadal dysgenesis with structural anomalies of the Y chromosomeS A Al-Awadi, T I Farag, D S Murthy, et al.
American Journal of Medical Genetics|August 1, 1983
Ullrich-Turner syndrome in monozygotic twinsS A Al-Awadi, A Cuschieri, T I Farag, et al.
Journal of Medical Genetics|February 1, 1986
Complex translocation involving chromosomes Y, 1, and 3 resulting in deletion of segment 3q23----q25S A Al-Awadi, K K Naguib, T I Farag, et al.
Clinical Genetics|May 1, 1985
Consanguinity among the Kuwaiti populationS A Al-Awadi, M A Moussa, K K Naguib, et al.
Journal of Medical Genetics|December 1, 1987
Unilateral true hermaphrodite with 46,XX/46,XY dispermic chimerismT I Farag, S A Al-Awadi, P Tippett, 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|June 1, 1984
Spondyloepiphyseal dysplasia tarda with progressive arthropathyS A Al-Awadi, T I Fårag, K Naguib, et al.
Annales De Genetique|January 1, 1987
Robertsonian translocation t dic (14p;22p) with regular trisomy 21: a possible interchromosomal effect?T I Farag, D S Krishna Murthy, S A Al-Awadi, et al.
American Journal of Medical Genetics|November 1, 1985
Primary hypogonadism and partial alopecia in three sibs with müllerian hypoplasia in the affected femalesS A Al-Awadi, T I Farag, A S Teebi, et al.
Pageof 9

Showing results (61-70 of 87) with videos related to

Sort By:
Pageof 9
American Journal of Medical Genetics|June 1, 1989
Familial uterine hernia syndrome: report of an Arab family with four affected malesK K Naguib, A S Teebi, T I Farag, et al.
Annals of Saudi Medicine|May 1, 1994
Mixed gonadal dysgenesis with structural anomalies of the Y chromosomeS A Al-Awadi, T I Farag, D S Murthy, et al.
American Journal of Medical Genetics|August 1, 1983
Ullrich-Turner syndrome in monozygotic twinsS A Al-Awadi, A Cuschieri, T I Farag, et al.
Journal of Medical Genetics|February 1, 1986
Complex translocation involving chromosomes Y, 1, and 3 resulting in deletion of segment 3q23----q25S A Al-Awadi, K K Naguib, T I Farag, et al.
Clinical Genetics|May 1, 1985
Consanguinity among the Kuwaiti populationS A Al-Awadi, M A Moussa, K K Naguib, et al.
Journal of Medical Genetics|December 1, 1987
Unilateral true hermaphrodite with 46,XX/46,XY dispermic chimerismT I Farag, S A Al-Awadi, P Tippett, 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|June 1, 1984
Spondyloepiphyseal dysplasia tarda with progressive arthropathyS A Al-Awadi, T I Fårag, K Naguib, et al.
Annales De Genetique|January 1, 1987
Robertsonian translocation t dic (14p;22p) with regular trisomy 21: a possible interchromosomal effect?T I Farag, D S Krishna Murthy, S A Al-Awadi, et al.
American Journal of Medical Genetics|November 1, 1985
Primary hypogonadism and partial alopecia in three sibs with müllerian hypoplasia in the affected femalesS A Al-Awadi, T I Farag, A S Teebi, et al.
Pageof 9