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American Journal of Medical Genetics
|
May 1, 1983
The campomelic syndrome: review, report of 17 cases, and follow-up on the currently 17-year-old boy first reported by Maroteaux et al in 1971
C S Houston, J M Opitz, J W Spranger, et al.
Zeitschrift Fur Kinderheilkunde
|
January 1, 1974
Generalized lymphangiectosis associated with chylothorax; a possible dysplasia of the lymphatic system
C K Chang, C Viseskul, J M Opitz, et al.
Birth Defects Original Article Series
|
January 1, 1987
The value of examining spontaneously aborted human embryos and placentas
H J Bruyere, S Arya, J S Kozel, et al.
American Journal of Medical Genetics
|
April 1, 1984
Tandem dup (1p) within the short arm of chromosome 1 in a child with ambiguous genitalia and multiple congenital anomalies
B R Elejalde, J M Opitz, M M de Elejalde, et al.
American Journal of Medical Genetics
|
November 1, 1983
A three-month-old infant with seizures, hypoglycemia, and apnea
R W Chesney, R J Sveum, M Lacey, et al.
American Journal of Medical Genetics
|
October 1, 1984
Fibrochondrogenesis: lethal, autosomal recessive chondrodysplasia with distinctive cartilage histopathology
C B Whitley, L O Langer, J Ophoven, et al.
The Journal of Pediatrics
|
March 1, 1984
Apnea and sudden unexpected death in infants with achondroplasia
R M Pauli, C I Scott, E R Wassman, et al.
American Journal of Medical Genetics
|
January 1, 1981
The dup(3q) syndrome: report of eight cases and review of the literature
P Steinbach, W N Adkins, H Caspar, et al.
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of 22
Search research articles
Search
Showing results (211-220 of 218) with videos related to
Sort By:
Page
of 22
You have reached the last page of results.
This site can display upto 218 results.
American Journal of Medical Genetics
|
May 1, 1983
The campomelic syndrome: review, report of 17 cases, and follow-up on the currently 17-year-old boy first reported by Maroteaux et al in 1971
C S Houston, J M Opitz, J W Spranger, et al.
Zeitschrift Fur Kinderheilkunde
|
January 1, 1974
Generalized lymphangiectosis associated with chylothorax; a possible dysplasia of the lymphatic system
C K Chang, C Viseskul, J M Opitz, et al.
Birth Defects Original Article Series
|
January 1, 1987
The value of examining spontaneously aborted human embryos and placentas
H J Bruyere, S Arya, J S Kozel, et al.
American Journal of Medical Genetics
|
April 1, 1984
Tandem dup (1p) within the short arm of chromosome 1 in a child with ambiguous genitalia and multiple congenital anomalies
B R Elejalde, J M Opitz, M M de Elejalde, et al.
American Journal of Medical Genetics
|
November 1, 1983
A three-month-old infant with seizures, hypoglycemia, and apnea
R W Chesney, R J Sveum, M Lacey, et al.
American Journal of Medical Genetics
|
October 1, 1984
Fibrochondrogenesis: lethal, autosomal recessive chondrodysplasia with distinctive cartilage histopathology
C B Whitley, L O Langer, J Ophoven, et al.
The Journal of Pediatrics
|
March 1, 1984
Apnea and sudden unexpected death in infants with achondroplasia
R M Pauli, C I Scott, E R Wassman, et al.
American Journal of Medical Genetics
|
January 1, 1981
The dup(3q) syndrome: report of eight cases and review of the literature
P Steinbach, W N Adkins, H Caspar, et al.
Page
of 22