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S A Al-Awadi

Showing results (71-80 of 87) with videos related to

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Journal of Medical Genetics|October 10, 1997
Unusual traits associated with Robinow syndromeM A Sabry, E A Ismail, R L al-Naggar, et al.
American Journal of Medical Genetics|December 1, 1992
Late diagnosis of phenylketonuria in a Bedouin motherR Usha, R Uma, T I Farag, et al.
American Journal of Medical Genetics|March 1, 1989
Direct duplication of chromosome 1, dir dup(1)(p21.2----p32) in a Bedouin boy with multiple congenital anomaliesF M Mohammed, T I Farag, S S Gunawardana, et al.
American Journal of Medical Genetics|April 1, 1988
Down syndrome and trisomy 18 in the BedouinsT I Farag, S A Al-Awadi, S A Al-Othman, et al.
Journal of Medical Genetics|January 1, 1993
The newly recognised limb/pelvis-hypoplasia/aplasia syndrome: report of a Bedouin patient and reviewT I Farag, S A al-Awadi, M J Marafie, et al.
Clinical Dysmorphology|May 18, 1999
New syndromic entity of situs inversus totalisM A Mubashir, M A Sabry, S Farah, et al.
Annales De Genetique|January 1, 1996
De novo direct duplication 7p (p11.2-->pter) in an Arab child with MCA/MR syndrome: trisomy 7p a delineated syndrome?M A Redha, D S Krishna Murthy, S A al-Awadi, et al.
Clinical Dysmorphology|May 8, 1998
Cutis verticis gyrata-mental deficiency syndrome: report of a case with unusual neuroradiological findingsS Farah, T Farag, M A Sabry, et al.
Clinical Genetics|October 1, 1992
Aminoacidopathies among institutionalised mentally retarded in KuwaitG Yadav, T I Farag, S A al Awadi, et al.
Clinical Genetics|March 5, 1999
Kenny-Caffey syndrome: an Arab variant?M A Sabry, T I Farag, A A Shaltout, et al.
Pageof 9

Showing results (71-80 of 87) with videos related to

Sort By:
Pageof 9
Journal of Medical Genetics|October 10, 1997
Unusual traits associated with Robinow syndromeM A Sabry, E A Ismail, R L al-Naggar, et al.
American Journal of Medical Genetics|December 1, 1992
Late diagnosis of phenylketonuria in a Bedouin motherR Usha, R Uma, T I Farag, et al.
American Journal of Medical Genetics|March 1, 1989
Direct duplication of chromosome 1, dir dup(1)(p21.2----p32) in a Bedouin boy with multiple congenital anomaliesF M Mohammed, T I Farag, S S Gunawardana, et al.
American Journal of Medical Genetics|April 1, 1988
Down syndrome and trisomy 18 in the BedouinsT I Farag, S A Al-Awadi, S A Al-Othman, et al.
Journal of Medical Genetics|January 1, 1993
The newly recognised limb/pelvis-hypoplasia/aplasia syndrome: report of a Bedouin patient and reviewT I Farag, S A al-Awadi, M J Marafie, et al.
Clinical Dysmorphology|May 18, 1999
New syndromic entity of situs inversus totalisM A Mubashir, M A Sabry, S Farah, et al.
Annales De Genetique|January 1, 1996
De novo direct duplication 7p (p11.2-->pter) in an Arab child with MCA/MR syndrome: trisomy 7p a delineated syndrome?M A Redha, D S Krishna Murthy, S A al-Awadi, et al.
Clinical Dysmorphology|May 8, 1998
Cutis verticis gyrata-mental deficiency syndrome: report of a case with unusual neuroradiological findingsS Farah, T Farag, M A Sabry, et al.
Clinical Genetics|October 1, 1992
Aminoacidopathies among institutionalised mentally retarded in KuwaitG Yadav, T I Farag, S A al Awadi, et al.
Clinical Genetics|March 5, 1999
Kenny-Caffey syndrome: an Arab variant?M A Sabry, T I Farag, A A Shaltout, et al.
Pageof 9