Related Experiment Videos

[Clinical polymorphism and various questions concerning the pathogenesis of multiple exostotic chondrodysplasia]

A A Razzokov, M A Berglezov, E M Meerson

Ortopediia Travmatologiia I Protezirovanie

|November 1, 1986

Abstract

No abstract available in PubMed .

Related Concept Videos

Articles linked to this work by shared authors, journal, and citation graph.

A missense mutation of C1659 in the fibroblast growth factor receptor 3 gene in Russian patients with hypochondroplasia.

Endocrine journal·1999

[Molecular-genetic characteristics of the deleted region of chromosome 8q24.1 in Langer-Giedion and tricho-rhino-phalangeal type I syndromes].

Genetika·1996

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 dysplasia.

Human mutation·1994

[Morphofunctional aspects of genetic analysis of osteogenesis imperfecta in cultured skin fibroblasts].

Biulleten' eksperimental'noi biologii i meditsiny·1992

[Current approaches to the development of a system of automated diagnosis of osteochondrodysplasias in children].

Ortopediia travmatologiia i protezirovanie·1991

[Pathogenetic aspects of studying clonal properties of bone marrow stromal cells in diseases of the osteoarticular system].

Ortopediia travmatologiia i protezirovanie·1990

See all related articles