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P Beighton

Showing results (161-170 of 292) with videos related to

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BDJ Open|April 18, 2019
Dentinogenesis imperfecta in Osteogenesis imperfecta type XI in South Africa: a genotype-phenotype correlationM Chetty, T Roberts, S Shaik, et al.
Clinical Genetics|July 1, 1983
The epidemiology of conjoined twinning in Southern AfricaD L Viljoen, M M Nelson, P Beighton
Clinical Genetics|November 1, 1993
Retinitis pigmentosa in southern AfricaJ Greenberg, L Bartmann, R Ramesar, et al.
Clinical Genetics|September 1, 1987
Ehlers-Danlos syndrome: yet another type?D Viljoen, J Goldblatt, D Thompson, et al.
Journal of Medical Genetics|June 1, 1979
Inherited anaemias in the Greek community of Cape TownR P Bonafede, M C Botha, P Beighton
Clinical Genetics|January 1, 1977
Sclerosteosis - an autosomal recessive disorderP Beighton, J Davidson, L Durr, et al.
Archives of Dermatology|June 1, 1971
Acquired cutis laxa. Primary generalized elastolysisW B Reed, R E Horowitz, P Beighton
American Journal of Medical Genetics|July 1, 1993
Brachydactylous dwarfs of MseleniD Viljoen, V Fredlund, R Ramesar, et al.
Clinical Genetics|May 1, 1989
Radial ray defects and associated anomaliesH Cox, D Viljoen, G Versfeld, et al.
Clinical Genetics|June 1, 1992
Retinitis pigmentosa, AD type I: exclusion of linkage to D3S47 (C17) in a large South African family of British originJ Greenberg, M Babaya, R Ramesar, et al.
Pageof 30

Showing results (161-170 of 292) with videos related to

Sort By:
Pageof 30
BDJ Open|April 18, 2019
Dentinogenesis imperfecta in Osteogenesis imperfecta type XI in South Africa: a genotype-phenotype correlationM Chetty, T Roberts, S Shaik, et al.
Clinical Genetics|July 1, 1983
The epidemiology of conjoined twinning in Southern AfricaD L Viljoen, M M Nelson, P Beighton
Clinical Genetics|November 1, 1993
Retinitis pigmentosa in southern AfricaJ Greenberg, L Bartmann, R Ramesar, et al.
Clinical Genetics|September 1, 1987
Ehlers-Danlos syndrome: yet another type?D Viljoen, J Goldblatt, D Thompson, et al.
Journal of Medical Genetics|June 1, 1979
Inherited anaemias in the Greek community of Cape TownR P Bonafede, M C Botha, P Beighton
Clinical Genetics|January 1, 1977
Sclerosteosis - an autosomal recessive disorderP Beighton, J Davidson, L Durr, et al.
Archives of Dermatology|June 1, 1971
Acquired cutis laxa. Primary generalized elastolysisW B Reed, R E Horowitz, P Beighton
American Journal of Medical Genetics|July 1, 1993
Brachydactylous dwarfs of MseleniD Viljoen, V Fredlund, R Ramesar, et al.
Clinical Genetics|May 1, 1989
Radial ray defects and associated anomaliesH Cox, D Viljoen, G Versfeld, et al.
Clinical Genetics|June 1, 1992
Retinitis pigmentosa, AD type I: exclusion of linkage to D3S47 (C17) in a large South African family of British originJ Greenberg, M Babaya, R Ramesar, et al.
Pageof 30