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American Journal of Human Genetics
|
February 1, 1993
Molecular analyses of a tyrosinase-negative albino family
K C Park, C D Chintamaneni, R Halaban, et al.
Birth Defects Original Article Series
|
June 1, 1971
Classification of albinism in man
C J Witkop, J G White, W E Nance, et al.
Scandinavian Journal of Haematology
|
March 1, 1977
The Hermansky-Pudlak syndrome. Evidence for a lowered 5-hydroxytryptamine content in platelets of heterozygotes
S M Gerritsen, J W Akkerman, B Nijmeijer, et al.
The American Journal of Medicine
|
March 1, 1987
Elevated urinary dolichol excretion in the Hermansky-Pudlak syndrome. Indicator of lysosomal dysfunction
C J Witkop, L S Wolfe, S X Cal, et al.
American Journal of Human Genetics
|
July 1, 1979
Hereditary mucoepithelial dysplasia: a disease apparently of desmosome and gap junction formation
C J Witkop, J G White, R A King, et al.
American Journal of Hematology
|
December 1, 1993
Synergistic effect of storage pool deficient platelets and low plasma von Willebrand factor on the severity of the hemorrhagic diathesis in Hermansky-Pudlak syndrome
C J Witkop, E J Bowie, M D Krumwiede, et al.
American Journal of Ophthalmology
|
April 15, 1991
Variable expression of albinism within a single kindred
S Castronuovo, J W Simon, G L Kandel, et al.
Birth Defects Original Article Series
|
January 11, 1975
The Saethre-Chotzen syndrome
O A Pantke, M M Cohen, C J Witkop, et al.
American Journal of Human Genetics
|
January 1, 1993
A frequent tyrosinase gene mutation associated with type I-A (tyrosinase-negative) oculocutaneous albinism in Puerto Rico
W S Oetting, C J Witkop, S A Brown, et al.
The Journal of Laboratory and Clinical Medicine
|
April 1, 1994
Pathogenesis of pulmonary fibrosis: platelet-derived growth factor precedes structural alterations in the Hermansky-Pudlak syndrome
K R Harmon, C J Witkop, J G White, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 62) with videos related to
Sort By:
Page
of 7
American Journal of Human Genetics
|
February 1, 1993
Molecular analyses of a tyrosinase-negative albino family
K C Park, C D Chintamaneni, R Halaban, et al.
Birth Defects Original Article Series
|
June 1, 1971
Classification of albinism in man
C J Witkop, J G White, W E Nance, et al.
Scandinavian Journal of Haematology
|
March 1, 1977
The Hermansky-Pudlak syndrome. Evidence for a lowered 5-hydroxytryptamine content in platelets of heterozygotes
S M Gerritsen, J W Akkerman, B Nijmeijer, et al.
The American Journal of Medicine
|
March 1, 1987
Elevated urinary dolichol excretion in the Hermansky-Pudlak syndrome. Indicator of lysosomal dysfunction
C J Witkop, L S Wolfe, S X Cal, et al.
American Journal of Human Genetics
|
July 1, 1979
Hereditary mucoepithelial dysplasia: a disease apparently of desmosome and gap junction formation
C J Witkop, J G White, R A King, et al.
American Journal of Hematology
|
December 1, 1993
Synergistic effect of storage pool deficient platelets and low plasma von Willebrand factor on the severity of the hemorrhagic diathesis in Hermansky-Pudlak syndrome
C J Witkop, E J Bowie, M D Krumwiede, et al.
American Journal of Ophthalmology
|
April 15, 1991
Variable expression of albinism within a single kindred
S Castronuovo, J W Simon, G L Kandel, et al.
Birth Defects Original Article Series
|
January 11, 1975
The Saethre-Chotzen syndrome
O A Pantke, M M Cohen, C J Witkop, et al.
American Journal of Human Genetics
|
January 1, 1993
A frequent tyrosinase gene mutation associated with type I-A (tyrosinase-negative) oculocutaneous albinism in Puerto Rico
W S Oetting, C J Witkop, S A Brown, et al.
The Journal of Laboratory and Clinical Medicine
|
April 1, 1994
Pathogenesis of pulmonary fibrosis: platelet-derived growth factor precedes structural alterations in the Hermansky-Pudlak syndrome
K R Harmon, C J Witkop, J G White, et al.
Page
of 7