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Birth Defects Original Article Series
|
January 1, 1975
Probable Marden-Walker syndrome: evidence for autosomal recessive inheritance
S A Temtamy, A S Shoukry, M Raafat, et al.
Birth Defects Original Article Series
|
January 1, 1975
Limb malformations in the cloverleaf skull anomaly
S A Temtamy, A S Shoukry, I Fayad, et al.
Clinical Dysmorphology
|
November 21, 1998
A new multiple congenital anomaly, mental retardation syndrome with preaxial brachydactyly, hyperphalangism, deafness and orodental anomalies
S A Temtamy, N A Meguid, S I Ismail, et al.
The Journal of the Egyptian Public Health Association
|
January 1, 1990
Heterozygous expression of Lesch-Nyhan syndrome clinical and ultrastructural studies
N A Meguid, E H Aboul-Ezz, E Seif, et al.
Genetic Counseling (Geneva, Switzerland)
|
May 23, 2012
Clinical and cytogenetic study of a case with familial chromosomal translocation presenting with facial dysmorphism and axial neuropathy
H T El-Bassyouni, M Shehab, H M Kora, et al.
Clinical Genetics
|
January 10, 2003
A novel point mutation of the androgen receptor (F804L) in an Egyptian newborn with complete androgen insensitivity associated with congenital glaucoma and hypertrophic pyloric stenosis
Y Z Gad, I Mazen, S Lumbroso, et al.
The Journal of Pediatrics
|
February 1, 1977
A postaxial polydactyly-dental-vertebral syndrome
J G Rogers, L S Levin, J P Dorst, et al.
Human Heredity
|
January 1, 1987
Familial Leydig cell hypoplasia as a cause of male pseudohermaphroditism
M K el-Awady, S A Temtamy, M A Salam, et al.
Genetic Counseling (Geneva, Switzerland)
|
April 23, 2005
Unusual pattern of inheritance and orodental changes in the Ellis-van Creveld syndrome
M I Mostafa, S A Temtamy, M A el-Gammal, et al.
Clinical Genetics
|
August 1, 1997
GAPO syndrome: first Egyptian case with ultrastructural changes in the gingiva
N A Meguid, H H Afifi, M I Ramzy, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 42) with videos related to
Sort By:
Page
of 5
Birth Defects Original Article Series
|
January 1, 1975
Probable Marden-Walker syndrome: evidence for autosomal recessive inheritance
S A Temtamy, A S Shoukry, M Raafat, et al.
Birth Defects Original Article Series
|
January 1, 1975
Limb malformations in the cloverleaf skull anomaly
S A Temtamy, A S Shoukry, I Fayad, et al.
Clinical Dysmorphology
|
November 21, 1998
A new multiple congenital anomaly, mental retardation syndrome with preaxial brachydactyly, hyperphalangism, deafness and orodental anomalies
S A Temtamy, N A Meguid, S I Ismail, et al.
The Journal of the Egyptian Public Health Association
|
January 1, 1990
Heterozygous expression of Lesch-Nyhan syndrome clinical and ultrastructural studies
N A Meguid, E H Aboul-Ezz, E Seif, et al.
Genetic Counseling (Geneva, Switzerland)
|
May 23, 2012
Clinical and cytogenetic study of a case with familial chromosomal translocation presenting with facial dysmorphism and axial neuropathy
H T El-Bassyouni, M Shehab, H M Kora, et al.
Clinical Genetics
|
January 10, 2003
A novel point mutation of the androgen receptor (F804L) in an Egyptian newborn with complete androgen insensitivity associated with congenital glaucoma and hypertrophic pyloric stenosis
Y Z Gad, I Mazen, S Lumbroso, et al.
The Journal of Pediatrics
|
February 1, 1977
A postaxial polydactyly-dental-vertebral syndrome
J G Rogers, L S Levin, J P Dorst, et al.
Human Heredity
|
January 1, 1987
Familial Leydig cell hypoplasia as a cause of male pseudohermaphroditism
M K el-Awady, S A Temtamy, M A Salam, et al.
Genetic Counseling (Geneva, Switzerland)
|
April 23, 2005
Unusual pattern of inheritance and orodental changes in the Ellis-van Creveld syndrome
M I Mostafa, S A Temtamy, M A el-Gammal, et al.
Clinical Genetics
|
August 1, 1997
GAPO syndrome: first Egyptian case with ultrastructural changes in the gingiva
N A Meguid, H H Afifi, M I Ramzy, et al.
Page
of 5