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Human Genetics
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July 1, 1997
Expanded CAG repeats in spinocerebellar ataxia (SCA1) segregate with distinct haplotypes in South african families
R S Ramesar, S Bardien, P Beighton, et al.
Journal of Medical Genetics
|
October 1, 1986
Mutations linked to the pro alpha 2(I) collagen gene are responsible for several cases of osteogenesis imperfecta type I
G Wallis, P Beighton, C Boyd, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
November 21, 1987
Morquio's disease type B (beta-galactosidase deficiency) in three siblings
M Beck, E M Petersen, J Spranger, et al.
Skeletal Radiology
|
August 18, 1999
Broad clavicles in trisomy 8 mosaicism: a new sign
P Beighton, K S Kozlowski, J Gardner, et al.
Pediatric Radiology
|
January 1, 1994
Bone dysplasias of infancy in the Vienna collection
P Beighton, E Sujansky, B Patzak, et al.
Clinical Orthopaedics and Related Research
|
March 1, 1984
Collagen defect of bone in osteogenesis imperfecta (Type I). An electron microscopic study
C J Jones, C Cummings, J Ball, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
May 11, 1974
Transkei foot
P A Schwartz, D Shlugman, G Daynes, et al.
The Journal of Clinical Pediatric Dentistry
|
February 19, 2004
Dental implications of Tooth-Nail dysplasia (Witkop syndrome): a report of an affected family and an approach to dental management
G M Wicomb, L X G Stephen, P Beighton
Annals of the Rheumatic Diseases
|
July 1, 1973
Serum uric acid concentrations in a rural Tswana community in Southern Africa
P Beighton, L Solomon, C L Soskolne, et al.
Annals of the New York Academy of Sciences
|
January 1, 1991
Profound childhood deafness in southern Africa
P Beighton, D Viljoen, I Winship, et al.
Page
of 30
Search research articles
Search
Showing results (201-210 of 292) with videos related to
Sort By:
Page
of 30
Human Genetics
|
July 1, 1997
Expanded CAG repeats in spinocerebellar ataxia (SCA1) segregate with distinct haplotypes in South african families
R S Ramesar, S Bardien, P Beighton, et al.
Journal of Medical Genetics
|
October 1, 1986
Mutations linked to the pro alpha 2(I) collagen gene are responsible for several cases of osteogenesis imperfecta type I
G Wallis, P Beighton, C Boyd, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
November 21, 1987
Morquio's disease type B (beta-galactosidase deficiency) in three siblings
M Beck, E M Petersen, J Spranger, et al.
Skeletal Radiology
|
August 18, 1999
Broad clavicles in trisomy 8 mosaicism: a new sign
P Beighton, K S Kozlowski, J Gardner, et al.
Pediatric Radiology
|
January 1, 1994
Bone dysplasias of infancy in the Vienna collection
P Beighton, E Sujansky, B Patzak, et al.
Clinical Orthopaedics and Related Research
|
March 1, 1984
Collagen defect of bone in osteogenesis imperfecta (Type I). An electron microscopic study
C J Jones, C Cummings, J Ball, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
May 11, 1974
Transkei foot
P A Schwartz, D Shlugman, G Daynes, et al.
The Journal of Clinical Pediatric Dentistry
|
February 19, 2004
Dental implications of Tooth-Nail dysplasia (Witkop syndrome): a report of an affected family and an approach to dental management
G M Wicomb, L X G Stephen, P Beighton
Annals of the Rheumatic Diseases
|
July 1, 1973
Serum uric acid concentrations in a rural Tswana community in Southern Africa
P Beighton, L Solomon, C L Soskolne, et al.
Annals of the New York Academy of Sciences
|
January 1, 1991
Profound childhood deafness in southern Africa
P Beighton, D Viljoen, I Winship, et al.
Page
of 30