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J W Spranger

Showing results (21-30 of 46) with videos related to

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Humangenetik|January 1, 1971
Heterogeneity of Chondrodysplasia punctataJ W Spranger, J M Opitz, U Bidder
Lancet (London, England)|April 16, 1977
Epiphyseal cartilage chemistry in thanatophoric dwarfismA C Sewell, J W Spranger, C A Pennock
The New England Journal of Medicine|March 9, 1972
The Stickler syndromeJ M Opitz, T France, J Herrmann, et al.
Birth Defects Original Article Series|January 1, 1974
The campomelic syndrome--commentsJ M Opitz, M Feingold, M J Bull, et al.
American Journal of Medical Genetics. Part A|November 20, 2004
A disorder resembling pseudoachondroplasia but without COMP mutationJ W Spranger, B Zabel, J Kennedy, et al.
Birth Defects Original Article Series|January 1, 1975
The Stickler syndrome (hereditary arthroophthalmopathy)J Herrmann, T D France, J W Spranger, et al.
American Journal of Medical Genetics|October 23, 1997
Vitamin K deficiency embryopathy: a phenocopy of the warfarin embryopathy due to a disorder of embryonic vitamin K metabolismH Menger, A E Lin, H V Toriello, et al.
American Journal of Medical Genetics|January 1, 1979
Developmental terms -- some proposals: first report of an international working groupK Benirschke, R B Lowry, J M Opitz, et al.
American Journal of Medical Genetics|March 1, 1987
Sedaghatian congenital lethal metaphyseal chondrodysplasia--observations in a second Iranian family and histopathological studiesJ M Opitz, J W Spranger, H R Stöss, et al.
American Journal of Medical Genetics. Part A|February 3, 2004
A new type of autosomal recessive spondyloepiphyseal dysplasia tardaJ G Leroy, B P Leroy, L V Emmery, et al.
Pageof 5

Showing results (21-30 of 46) with videos related to

Sort By:
Pageof 5
Humangenetik|January 1, 1971
Heterogeneity of Chondrodysplasia punctataJ W Spranger, J M Opitz, U Bidder
Lancet (London, England)|April 16, 1977
Epiphyseal cartilage chemistry in thanatophoric dwarfismA C Sewell, J W Spranger, C A Pennock
The New England Journal of Medicine|March 9, 1972
The Stickler syndromeJ M Opitz, T France, J Herrmann, et al.
Birth Defects Original Article Series|January 1, 1974
The campomelic syndrome--commentsJ M Opitz, M Feingold, M J Bull, et al.
American Journal of Medical Genetics. Part A|November 20, 2004
A disorder resembling pseudoachondroplasia but without COMP mutationJ W Spranger, B Zabel, J Kennedy, et al.
Birth Defects Original Article Series|January 1, 1975
The Stickler syndrome (hereditary arthroophthalmopathy)J Herrmann, T D France, J W Spranger, et al.
American Journal of Medical Genetics|October 23, 1997
Vitamin K deficiency embryopathy: a phenocopy of the warfarin embryopathy due to a disorder of embryonic vitamin K metabolismH Menger, A E Lin, H V Toriello, et al.
American Journal of Medical Genetics|January 1, 1979
Developmental terms -- some proposals: first report of an international working groupK Benirschke, R B Lowry, J M Opitz, et al.
American Journal of Medical Genetics|March 1, 1987
Sedaghatian congenital lethal metaphyseal chondrodysplasia--observations in a second Iranian family and histopathological studiesJ M Opitz, J W Spranger, H R Stöss, et al.
American Journal of Medical Genetics. Part A|February 3, 2004
A new type of autosomal recessive spondyloepiphyseal dysplasia tardaJ G Leroy, B P Leroy, L V Emmery, et al.
Pageof 5