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Medical Principles and Practice : International Journal of the Kuwait University, Health Science Centre
|
October 2, 2013
Connexin 26 gene mutations in non-syndromic hearing loss among Kuwaiti patients
Khalid Al-Sebeih, Marium Al-Kandari, Sadika 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 females
S A Al-Awadi, T I Farag, A S Teebi, et al.
Journal of Medical Genetics
|
October 10, 1997
Unusual traits associated with Robinow syndrome
M 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 mother
R 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 anomalies
F M Mohammed, T I Farag, S S Gunawardana, et al.
Journal of Medical Genetics
|
January 1, 1993
The newly recognised limb/pelvis-hypoplasia/aplasia syndrome: report of a Bedouin patient and review
T I Farag, S A al-Awadi, M J Marafie, et al.
Clinical Dysmorphology
|
May 18, 1999
New syndromic entity of situs inversus totalis
M A Mubashir, M A Sabry, S Farah, et al.
The Journal of the Egyptian Public Health Association
|
June 5, 2009
Cytogenetic Abnormalities and Herdetiry Thrombophilias among the Abortees:
Alaa E Elshafaay, Fawziah M Mostafa, Sadica A Al-Awadi, 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 findings
S Farah, T Farag, M A Sabry, et al.
Page
of 13
Search research articles
Search
Showing results (101-110 of 123) with videos related to
Sort By:
Page
of 13
Medical Principles and Practice : International Journal of the Kuwait University, Health Science Centre
|
October 2, 2013
Connexin 26 gene mutations in non-syndromic hearing loss among Kuwaiti patients
Khalid Al-Sebeih, Marium Al-Kandari, Sadika 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 females
S A Al-Awadi, T I Farag, A S Teebi, et al.
Journal of Medical Genetics
|
October 10, 1997
Unusual traits associated with Robinow syndrome
M 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 mother
R 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 anomalies
F M Mohammed, T I Farag, S S Gunawardana, et al.
Journal of Medical Genetics
|
January 1, 1993
The newly recognised limb/pelvis-hypoplasia/aplasia syndrome: report of a Bedouin patient and review
T I Farag, S A al-Awadi, M J Marafie, et al.
Clinical Dysmorphology
|
May 18, 1999
New syndromic entity of situs inversus totalis
M A Mubashir, M A Sabry, S Farah, et al.
The Journal of the Egyptian Public Health Association
|
June 5, 2009
Cytogenetic Abnormalities and Herdetiry Thrombophilias among the Abortees:
Alaa E Elshafaay, Fawziah M Mostafa, Sadica A Al-Awadi, 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 findings
S Farah, T Farag, M A Sabry, et al.
Page
of 13