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E M Meerson

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Ortopediia Travmatologiia I Protezirovanie|December 1, 1977
[Various rare forms of dysostoses]M V Volkov, E M Meerson, G P Iukina, et al.
Ortopediia Travmatologiia I Protezirovanie|November 1, 1986
[Clinical polymorphism and various questions concerning the pathogenesis of multiple exostotic chondrodysplasia]A A Razzokov, M A Berglezov, E M Meerson, et al.
Genetika|July 1, 1996
[Molecular-genetic characteristics of the deleted region of chromosome 8q24.1 in Langer-Giedion and tricho-rhino-phalangeal type I syndromes]M V Nemtsova, A N Iatsenko, N P Kuleshov, et al.
Human Mutation|January 1, 1994
A single base mutation in the type II procollagen gene (COL2A1) that converts glycine alpha 1-247 to serine in a family with late-onset spondyloepiphyseal dysplasiaP Ritvaniemi, B P Sokolov, C J Williams, et al.
Biulleten' Eksperimental'Noi Biologii I Meditsiny|July 1, 1992
[Morphofunctional aspects of genetic analysis of osteogenesis imperfecta in cultured skin fibroblasts]E M Meerson, F S Barer, A P Berezhnyĭ, et al.
Ortopediia Travmatologiia I Protezirovanie|September 1, 1990
[Pathogenetic aspects of studying clonal properties of bone marrow stromal cells in diseases of the osteoarticular system]E M Meerson, V K Il'ina, F S Barer, et al.
Endocrine Journal|July 8, 1999
A missense mutation of C1659 in the fibroblast growth factor receptor 3 gene in Russian patients with hypochondroplasiaO V Fofanova, N Takamura, E Kinoshita, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Ortopediia Travmatologiia I Protezirovanie|December 1, 1977
[Various rare forms of dysostoses]M V Volkov, E M Meerson, G P Iukina, et al.
Ortopediia Travmatologiia I Protezirovanie|November 1, 1986
[Clinical polymorphism and various questions concerning the pathogenesis of multiple exostotic chondrodysplasia]A A Razzokov, M A Berglezov, E M Meerson, et al.
Genetika|July 1, 1996
[Molecular-genetic characteristics of the deleted region of chromosome 8q24.1 in Langer-Giedion and tricho-rhino-phalangeal type I syndromes]M V Nemtsova, A N Iatsenko, N P Kuleshov, et al.
Human Mutation|January 1, 1994
A single base mutation in the type II procollagen gene (COL2A1) that converts glycine alpha 1-247 to serine in a family with late-onset spondyloepiphyseal dysplasiaP Ritvaniemi, B P Sokolov, C J Williams, et al.
Biulleten' Eksperimental'Noi Biologii I Meditsiny|July 1, 1992
[Morphofunctional aspects of genetic analysis of osteogenesis imperfecta in cultured skin fibroblasts]E M Meerson, F S Barer, A P Berezhnyĭ, et al.
Ortopediia Travmatologiia I Protezirovanie|September 1, 1990
[Pathogenetic aspects of studying clonal properties of bone marrow stromal cells in diseases of the osteoarticular system]E M Meerson, V K Il'ina, F S Barer, et al.
Endocrine Journal|July 8, 1999
A missense mutation of C1659 in the fibroblast growth factor receptor 3 gene in Russian patients with hypochondroplasiaO V Fofanova, N Takamura, E Kinoshita, et al.
Pageof 3