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S A al-Awadi

Showing results (11-20 of 87) with videos related to

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Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|March 1, 1986
De novo partial monosomy 21 with unusual karyotypeS A Al-Awadi, K K Naguib, A S Teebi, et al.
American Journal of Medical Genetics|April 15, 1994
Autosomal recessive congenital diaphragmatic defects in the ArabsT I Farag, L Bastaki, M Marafie, et al.
Indian Journal of Pediatrics|March 1, 1990
Familial fragile secondary constriction on chromosome 2 (2q11) with unusual features and psychomotor retardationD S Murthy, A S Teebi, T S Sundareshan, et al.
Journal of the Royal Society of Medicine|July 1, 1981
Familial jejunal atresia with 'apple-peel' variantS A Al-Awadi, T I Farag, K Naguib, et al.
Journal of Medical Genetics|October 1, 1987
Brachmann-de Lange syndrome in sibsK K Naguib, A S Teebi, S A Al-Awadi, et al.
American Journal of Medical Genetics|June 1, 1986
Hypogonadotropic hypogonadism, mental retardation, obesity and minor skeletal abnormalities: another new autosomal recessive syndrome from the Middle EastA S Teebi, S A Al-Awadi, T I Farag, et al.
American Journal of Medical Genetics|July 1, 1990
Penile enlargement in 3q23-q25 deletion syndromeK K Naguib, S A al-Awadi, T I Farag, et al.
Journal of Medical Genetics|June 1, 1987
Hypoplastic tibiae with postaxial polysyndactyly: a new dominant syndrome?S A Al-Awadi, K K Naguib, T I Farag, et al.
Indian Journal of Pediatrics|March 1, 1988
Trisomy 4q: 46, xy,-11, +der (11), t(4;11) (q27; q25) pat in a child with multiple congenital anomaliesS A al-Awadi, K K Naguib, S A al-Othman, et al.
American Journal of Medical Genetics|February 7, 1998
Lowry-Maclean syndrome with osteopenic bones and possible autosomal dominant inheritance in a Bedouin familyN A Al-Torki, M A Sabry, S A Al-Awadi, et al.
Pageof 9

Showing results (11-20 of 87) with videos related to

Sort By:
Pageof 9
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|March 1, 1986
De novo partial monosomy 21 with unusual karyotypeS A Al-Awadi, K K Naguib, A S Teebi, et al.
American Journal of Medical Genetics|April 15, 1994
Autosomal recessive congenital diaphragmatic defects in the ArabsT I Farag, L Bastaki, M Marafie, et al.
Indian Journal of Pediatrics|March 1, 1990
Familial fragile secondary constriction on chromosome 2 (2q11) with unusual features and psychomotor retardationD S Murthy, A S Teebi, T S Sundareshan, et al.
Journal of the Royal Society of Medicine|July 1, 1981
Familial jejunal atresia with 'apple-peel' variantS A Al-Awadi, T I Farag, K Naguib, et al.
Journal of Medical Genetics|October 1, 1987
Brachmann-de Lange syndrome in sibsK K Naguib, A S Teebi, S A Al-Awadi, et al.
American Journal of Medical Genetics|June 1, 1986
Hypogonadotropic hypogonadism, mental retardation, obesity and minor skeletal abnormalities: another new autosomal recessive syndrome from the Middle EastA S Teebi, S A Al-Awadi, T I Farag, et al.
American Journal of Medical Genetics|July 1, 1990
Penile enlargement in 3q23-q25 deletion syndromeK K Naguib, S A al-Awadi, T I Farag, et al.
Journal of Medical Genetics|June 1, 1987
Hypoplastic tibiae with postaxial polysyndactyly: a new dominant syndrome?S A Al-Awadi, K K Naguib, T I Farag, et al.
Indian Journal of Pediatrics|March 1, 1988
Trisomy 4q: 46, xy,-11, +der (11), t(4;11) (q27; q25) pat in a child with multiple congenital anomaliesS A al-Awadi, K K Naguib, S A al-Othman, et al.
American Journal of Medical Genetics|February 7, 1998
Lowry-Maclean syndrome with osteopenic bones and possible autosomal dominant inheritance in a Bedouin familyN A Al-Torki, M A Sabry, S A Al-Awadi, et al.
Pageof 9