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Blood Cells, Molecules & Diseases
|
July 10, 2003
The 1226G (N370S) Gaucher mutation among patients with Legg-Calve-Perthes disease
G Kenet, S Hayek, M Mor, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
September 8, 2001
Gnathodiaphyseal dysplasia: a syndrome of fibro-osseous lesions of jawbones, bone fragility, and long bone bowing
M Riminucci, M T Collins, A Corsi, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
January 26, 2000
Mutations of the GNAS1 gene, stromal cell dysfunction, and osteomalacic changes in non-McCune-Albright fibrous dysplasia of bone
P Bianco, M Riminucci, A Majolagbe, et al.
Journal of Medical Genetics
|
May 17, 2005
Camurati-Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatment
K Janssens, F Vanhoenacker, M Bonduelle, et al.
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of 12
Search research articles
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Showing results (111-120 of 114) with videos related to
Sort By:
Page
of 12
You have reached the last page of results.
This site can display upto 114 results.
Blood Cells, Molecules & Diseases
|
July 10, 2003
The 1226G (N370S) Gaucher mutation among patients with Legg-Calve-Perthes disease
G Kenet, S Hayek, M Mor, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
September 8, 2001
Gnathodiaphyseal dysplasia: a syndrome of fibro-osseous lesions of jawbones, bone fragility, and long bone bowing
M Riminucci, M T Collins, A Corsi, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
January 26, 2000
Mutations of the GNAS1 gene, stromal cell dysfunction, and osteomalacic changes in non-McCune-Albright fibrous dysplasia of bone
P Bianco, M Riminucci, A Majolagbe, et al.
Journal of Medical Genetics
|
May 17, 2005
Camurati-Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatment
K Janssens, F Vanhoenacker, M Bonduelle, et al.
Page
of 12