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Human Heredity
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July 1, 1995
Possible genetic heterogeneity in the Roberts-SC phocomelia syndrome
M A Sabry
Journal of Medical Genetics
|
November 1, 1994
The possible Middle East origin of the mutation for the limb/pelvis-hypoplasia/aplasia syndrome
M A Sabry
Journal of Muscle Research and Cell Motility
|
February 1, 1989
Identification and pattern of expression of a developmental isoform of troponin I in chicken and rat cardiac muscle
M A Sabry, G K Dhoot
Journal of Molecular and Cellular Cardiology
|
January 1, 1989
Identification of and changes in the expression of troponin T isoforms in developing avian and mammalian heart
M A Sabry, G K Dhoot
American Journal of Medical Genetics
|
April 24, 1996
Hand anomalies in fetal-hydantoin syndrome: from nail/phalangeal hypoplasia to unilateral acheiria
M A Sabry, T I Farag
Journal of Muscle Research and Cell Motility
|
October 1, 1991
Identification and pattern of transitions of some developmental and adult isoforms of fast troponin T in some human and rat skeletal muscles
M A Sabry, G K Dhoot
Journal of Muscle Research and Cell Motility
|
June 1, 1991
Identification of and pattern of transitions of cardiac, adult slow and slow skeletal muscle-like embryonic isoforms of troponin T in developing rat and human skeletal muscles
M A Sabry, G K Dhoot
Journal of Intellectual Disability Research : JIDR
|
July 25, 1998
Chromosome 15q11-13 region and the autistic disorder
M A Sabry, T I Farag
Journal of Medical Genetics
|
December 24, 1998
Genotypic/phenotypic heterogeneity of Kenny-Caffey syndrome
M A Sabry, M Zaki, A Shaltout
European Journal of Pediatrics
|
February 7, 1998
Nephrocalcinosis and urolithiasis in carbonic anhydrase II deficiency syndrome
E A Ismail, S Abul Saad, M A Sabry
Page
of 4
Search research articles
Search
Showing results (1-10 of 33) with videos related to
Sort By:
Page
of 4
Human Heredity
|
July 1, 1995
Possible genetic heterogeneity in the Roberts-SC phocomelia syndrome
M A Sabry
Journal of Medical Genetics
|
November 1, 1994
The possible Middle East origin of the mutation for the limb/pelvis-hypoplasia/aplasia syndrome
M A Sabry
Journal of Muscle Research and Cell Motility
|
February 1, 1989
Identification and pattern of expression of a developmental isoform of troponin I in chicken and rat cardiac muscle
M A Sabry, G K Dhoot
Journal of Molecular and Cellular Cardiology
|
January 1, 1989
Identification of and changes in the expression of troponin T isoforms in developing avian and mammalian heart
M A Sabry, G K Dhoot
American Journal of Medical Genetics
|
April 24, 1996
Hand anomalies in fetal-hydantoin syndrome: from nail/phalangeal hypoplasia to unilateral acheiria
M A Sabry, T I Farag
Journal of Muscle Research and Cell Motility
|
October 1, 1991
Identification and pattern of transitions of some developmental and adult isoforms of fast troponin T in some human and rat skeletal muscles
M A Sabry, G K Dhoot
Journal of Muscle Research and Cell Motility
|
June 1, 1991
Identification of and pattern of transitions of cardiac, adult slow and slow skeletal muscle-like embryonic isoforms of troponin T in developing rat and human skeletal muscles
M A Sabry, G K Dhoot
Journal of Intellectual Disability Research : JIDR
|
July 25, 1998
Chromosome 15q11-13 region and the autistic disorder
M A Sabry, T I Farag
Journal of Medical Genetics
|
December 24, 1998
Genotypic/phenotypic heterogeneity of Kenny-Caffey syndrome
M A Sabry, M Zaki, A Shaltout
European Journal of Pediatrics
|
February 7, 1998
Nephrocalcinosis and urolithiasis in carbonic anhydrase II deficiency syndrome
E A Ismail, S Abul Saad, M A Sabry
Page
of 4