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Genetic Counseling (Geneva, Switzerland)
|
January 13, 2000
A new case of neonatal progeroid syndrome with agenesis of corpus callosum
G M Abdel-Salam, A E Czeizel
Ophthalmic Genetics
|
January 5, 2000
Microcephaly with normal intelligence, and chorioretinopathy
G M Abdel-Salam, G Vogt, A Halász, et al.
Developmental Medicine and Child Neurology
|
December 5, 2000
Association of epilepsy with different groups of microcephaly
G M Abdel-Salam, A A Halász, A E Czeizel
American Journal of Medical Genetics
|
January 9, 2001
Microcephaly with chorioretinal dysplasia: characteristic facial features
G M Abdel-Salam, A E Czeizel, G Vogt, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 5, 2001
Microcephaly, microphthalmia, congenital cataract, with calcification of the basal ganglia: MCA/MR syndrome
G M Abdel-Salam, A Svékus, Z Pelle, et al.
Neurology
|
January 26, 2011
Distinguishing 3 classes of corpus callosal abnormalities in consanguineous families
R M Hanna, S E Marsh, D Swistun, et al.
Bratislavske Lekarske Listy
|
May 1, 2010
The most encountered groups of genetic disorders in Giza Governorate, Egypt
H H Afifi, M O El-Ruby, H T El-Bassyouni, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Genetic Counseling (Geneva, Switzerland)
|
January 13, 2000
A new case of neonatal progeroid syndrome with agenesis of corpus callosum
G M Abdel-Salam, A E Czeizel
Ophthalmic Genetics
|
January 5, 2000
Microcephaly with normal intelligence, and chorioretinopathy
G M Abdel-Salam, G Vogt, A Halász, et al.
Developmental Medicine and Child Neurology
|
December 5, 2000
Association of epilepsy with different groups of microcephaly
G M Abdel-Salam, A A Halász, A E Czeizel
American Journal of Medical Genetics
|
January 9, 2001
Microcephaly with chorioretinal dysplasia: characteristic facial features
G M Abdel-Salam, A E Czeizel, G Vogt, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 5, 2001
Microcephaly, microphthalmia, congenital cataract, with calcification of the basal ganglia: MCA/MR syndrome
G M Abdel-Salam, A Svékus, Z Pelle, et al.
Neurology
|
January 26, 2011
Distinguishing 3 classes of corpus callosal abnormalities in consanguineous families
R M Hanna, S E Marsh, D Swistun, et al.
Bratislavske Lekarske Listy
|
May 1, 2010
The most encountered groups of genetic disorders in Giza Governorate, Egypt
H H Afifi, M O El-Ruby, H T El-Bassyouni, et al.
Page
of 1