Tracing the pathway between mutation and phenotype in osteogenesis imperfecta: Isolation of mineralization-specific genes

American Journal of Medical Genetics

Volumn 63, Issue 1, 1996, Pages 167-174

  Culbert, Ainsley A ^a   Wallis, Gillian A ^a,b   Kadler, Karl E ^a  

^a UNIVERSITY OF MANCHESTER   (United Kingdom)

^b UNIVERSITY OF MANCHESTER   (United Kingdom)

Author keywords

bone; collagen; genes; osteogenesis imperfecta; RNA; subtraction

Indexed keywords

ALKALINE PHOSPHATASE; FIBRONECTIN; OSTEOPONTIN; SIALOPROTEIN;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CHICK EMBRYO; DNA LIBRARY; EMBRYO; GENE EXPRESSION; GENE MUTATION; HOUSEKEEPING GENE; MINERALIZATION; MOLECULAR CLONING; NONHUMAN; OSSIFICATION; OSTEOGENESIS IMPERFECTA; PHENOTYPE; PRIORITY JOURNAL; RNA ANALYSIS; SKIN FIBROBLAST;

ALKALINE PHOSPHATASE; ANIMALS; BASE SEQUENCE; CALCIFICATION, PHYSIOLOGIC; CHICK EMBRYO; CLONING, MOLECULAR; COLLAGEN; CYSTATINS; DNA PRIMERS; DNA PROBES; DNA, COMPLEMENTARY; FIBROBLASTS; FIBRONECTINS; GENE LIBRARY; HUMANS; MOLECULAR SEQUENCE DATA; OSTEOGENESIS IMPERFECTA; OSTEOPONTIN; PHENOTYPE; PHOSPHOPROTEINS; POLYMERASE CHAIN REACTION; RNA, MESSENGER; SIALOGLYCOPROTEINS; SKIN; SKIN PHYSIOLOGY; SKULL;

EID: 0029871327     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19960503)63:1<167::AID-AJMG29>3.0.CO;2-L     Document Type: Article

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