Search research articles
Contact Us
Filters
Showing results (21-30 of 51) with videos related to
Page
of 6
Sort By:
Pediatric Radiology
|
November 3, 1998
Extra pelvic ossification centers in thanatophoric dysplasia and platyspondylic lethal skeletal dysplasia-San Diego type
H Kitoh, R S Lachman, S G Brodie, et al.
Matrix Biology : Journal of the International Society for Matrix Biology
|
June 8, 2000
Exon skipping mutation in the COL9A2 gene in a family with multiple epiphyseal dysplasia
E C Spayde, A P Joshi, W R Wilcox, et al.
American Journal of Human Genetics
|
February 1, 1996
Atelosteogenesis type II is caused by mutations in the diastrophic dysplasia sulfate-transporter gene (DTDST): evidence for a phenotypic series involving three chondrodysplasias
J Hästbacka, A Superti-Furga, W R Wilcox, et al.
American Journal of Human Genetics
|
December 1, 1994
Expression, in cartilage, of a 7-amino-acid deletion in type II collagen from two unrelated individuals with Kniest dysplasia
R Bogaert, D Wilkin, W R Wilcox, et al.
American Journal of Medical Genetics
|
May 26, 1998
Pacman dysplasia: report of two affected sibs
W R Wilcox, B C Lucas, B Loebel, et al.
American Journal of Medical Genetics
|
December 18, 1998
Lethal osteosclerotic osteochondrodysplasia with platyspondyly, metaphyseal widening, and intracellular inclusions in sibs
S G Brodie, R S Lachman, A F Jewell, et al.
Matrix Biology : Journal of the International Society for Matrix Biology
|
November 20, 1998
Proteoglycan sulfation in cartilage and cell cultures from patients with sulfate transporter chondrodysplasias: relationship to clinical severity and indications on the role of intracellular sulfate production
A Rossi, I Kaitila, W R Wilcox, et al.
American Journal of Medical Genetics
|
June 9, 1999
Platyspondylic lethal skeletal dysplasia, San Diego type, is caused by FGFR3 mutations
S G Brodie, H Kitoh, R S Lachman, et al.
Human Mutation
|
July 29, 1999
Clinical spectrum of fibroblast growth factor receptor mutations
M R Passos-Bueno, W R Wilcox, E W Jabs, et al.
Nature Genetics
|
March 30, 2001
Dyssegmental dysplasia, Silverman-Handmaker type, is caused by functional null mutations of the perlecan gene
E Arikawa-Hirasawa, W R Wilcox, A H Le, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 51) with videos related to
Sort By:
Page
of 6
Pediatric Radiology
|
November 3, 1998
Extra pelvic ossification centers in thanatophoric dysplasia and platyspondylic lethal skeletal dysplasia-San Diego type
H Kitoh, R S Lachman, S G Brodie, et al.
Matrix Biology : Journal of the International Society for Matrix Biology
|
June 8, 2000
Exon skipping mutation in the COL9A2 gene in a family with multiple epiphyseal dysplasia
E C Spayde, A P Joshi, W R Wilcox, et al.
American Journal of Human Genetics
|
February 1, 1996
Atelosteogenesis type II is caused by mutations in the diastrophic dysplasia sulfate-transporter gene (DTDST): evidence for a phenotypic series involving three chondrodysplasias
J Hästbacka, A Superti-Furga, W R Wilcox, et al.
American Journal of Human Genetics
|
December 1, 1994
Expression, in cartilage, of a 7-amino-acid deletion in type II collagen from two unrelated individuals with Kniest dysplasia
R Bogaert, D Wilkin, W R Wilcox, et al.
American Journal of Medical Genetics
|
May 26, 1998
Pacman dysplasia: report of two affected sibs
W R Wilcox, B C Lucas, B Loebel, et al.
American Journal of Medical Genetics
|
December 18, 1998
Lethal osteosclerotic osteochondrodysplasia with platyspondyly, metaphyseal widening, and intracellular inclusions in sibs
S G Brodie, R S Lachman, A F Jewell, et al.
Matrix Biology : Journal of the International Society for Matrix Biology
|
November 20, 1998
Proteoglycan sulfation in cartilage and cell cultures from patients with sulfate transporter chondrodysplasias: relationship to clinical severity and indications on the role of intracellular sulfate production
A Rossi, I Kaitila, W R Wilcox, et al.
American Journal of Medical Genetics
|
June 9, 1999
Platyspondylic lethal skeletal dysplasia, San Diego type, is caused by FGFR3 mutations
S G Brodie, H Kitoh, R S Lachman, et al.
Human Mutation
|
July 29, 1999
Clinical spectrum of fibroblast growth factor receptor mutations
M R Passos-Bueno, W R Wilcox, E W Jabs, et al.
Nature Genetics
|
March 30, 2001
Dyssegmental dysplasia, Silverman-Handmaker type, is caused by functional null mutations of the perlecan gene
E Arikawa-Hirasawa, W R Wilcox, A H Le, et al.
Page
of 6