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Pediatric Cardiology
|
January 1, 1982
Congenital cardiac, pulmonary, and vascular malformations in oculoauriculovertebral dysplasia
M E Pierpont, J H Moller, R J Gorlin, et al.
Birth Defects Original Article Series
|
June 1, 1971
Frontonasal dysplasia (median cleft face syndrome): comments on etiology and pathogenesis
M M Cohen, H O Sedano, R J Gorlin, et al.
American Journal of Medical Genetics
|
October 11, 1992
Bannayan-Riley-Ruvalcaba syndrome
R J Gorlin, M M Cohen, L M Condon, et al.
Annales De Genetique
|
January 1, 1994
Clinical identification of a human equivalent to the short ear (se) murine phenotype
D Lacombe, A Toutain, R J Gorlin, et al.
The American Journal of Surgical Pathology
|
March 1, 1991
Melanotic neuroectodermal tumor of infancy. A reexamination of a histogenetic problem based on immunohistochemical, flow cytometric, and ultrastructural study of 10 cases
G Pettinato, J C Manivel, E S d'Amore, et al.
American Journal of Medical Genetics
|
December 11, 1996
Osteoglophonic dysplasia: review and further delineation of the syndrome
S Sklower Brooks, G Kassner, Q Qazi, et al.
Zeitschrift Fur Kinderheilkunde
|
January 1, 1974
Achondrogenesis within the scope of connately manifested generalized skeletal dysplasias
H R Wiedemann, W Remagen, H A Hienz, et al.
American Journal of Medical Genetics
|
May 15, 1994
Spondylocarpotarsal synostosis syndrome (with or without unilateral unsegmented bar)
L O Langer, R J Gorlin, D Donnai, et al.
American Journal of Medical Genetics
|
October 1, 1987
Acrocephalopolysyndactyly type II--Carpenter syndrome: clinical spectrum and an attempt at unification with Goodman and Summit syndromes
D M Cohen, J G Green, J Miller, et al.
Clinical Dysmorphology
|
January 1, 1993
Multiple circumferential skin folds and other anomalies: a problem in syndrome delineation
M M Cohen, R J Gorlin, R Clark, et al.
Page
of 25
Search research articles
Search
Showing results (181-190 of 246) with videos related to
Sort By:
Page
of 25
Pediatric Cardiology
|
January 1, 1982
Congenital cardiac, pulmonary, and vascular malformations in oculoauriculovertebral dysplasia
M E Pierpont, J H Moller, R J Gorlin, et al.
Birth Defects Original Article Series
|
June 1, 1971
Frontonasal dysplasia (median cleft face syndrome): comments on etiology and pathogenesis
M M Cohen, H O Sedano, R J Gorlin, et al.
American Journal of Medical Genetics
|
October 11, 1992
Bannayan-Riley-Ruvalcaba syndrome
R J Gorlin, M M Cohen, L M Condon, et al.
Annales De Genetique
|
January 1, 1994
Clinical identification of a human equivalent to the short ear (se) murine phenotype
D Lacombe, A Toutain, R J Gorlin, et al.
The American Journal of Surgical Pathology
|
March 1, 1991
Melanotic neuroectodermal tumor of infancy. A reexamination of a histogenetic problem based on immunohistochemical, flow cytometric, and ultrastructural study of 10 cases
G Pettinato, J C Manivel, E S d'Amore, et al.
American Journal of Medical Genetics
|
December 11, 1996
Osteoglophonic dysplasia: review and further delineation of the syndrome
S Sklower Brooks, G Kassner, Q Qazi, et al.
Zeitschrift Fur Kinderheilkunde
|
January 1, 1974
Achondrogenesis within the scope of connately manifested generalized skeletal dysplasias
H R Wiedemann, W Remagen, H A Hienz, et al.
American Journal of Medical Genetics
|
May 15, 1994
Spondylocarpotarsal synostosis syndrome (with or without unilateral unsegmented bar)
L O Langer, R J Gorlin, D Donnai, et al.
American Journal of Medical Genetics
|
October 1, 1987
Acrocephalopolysyndactyly type II--Carpenter syndrome: clinical spectrum and an attempt at unification with Goodman and Summit syndromes
D M Cohen, J G Green, J Miller, et al.
Clinical Dysmorphology
|
January 1, 1993
Multiple circumferential skin folds and other anomalies: a problem in syndrome delineation
M M Cohen, R J Gorlin, R Clark, et al.
Page
of 25