What is new in genetics and osteogenesis imperfecta classification?

Jornal de Pediatria

Volumn 90, Issue 6, 2014, Pages 536-541

  Valadares, Eugênia R ^a   Carneiro, Túlio B ^a   Santos, Paula M ^a,b   Oliveira, Ana Cristina ^a   Zabel, Bernhard ^a,b  

^a FEDERAL UNIVERSITY OF MINAS GERAIS   (Brazil)

^b UNIVERSITY OF FREIBURG   (Germany)

Author keywords

Collagen type 1; Osteochondrodysplasias; Osteogenesis imperfecta

Indexed keywords

BMP1 GENE; COL1A1 GENE; COL1A2 GENE; CRTAP GENE; DISEASE CLASSIFICATION; FKBP10 GENE; FRACTURE; GENE; GENE LOCUS; GENE MUTATION; GENETIC ASSOCIATION; GENETICS; HUMAN; INHERITANCE; LEPRE1 GENE; OSTEOGENESIS IMPERFECTA; OSTEOPOROSIS; PHENOTYPIC VARIATION; PLOD2 GENE; PPIB GENE; REVIEW; SERPINF1 GENE; SERPINH1 GENE; SP7 GENE; TMEM38B GENE; WNT1 GENE; CLASSIFICATION; MUTATION; PHYSIOLOGY;

COLLAGEN TYPE 1;

COLLAGEN TYPE I; HUMANS; MUTATION; OSTEOGENESIS IMPERFECTA;

EID: 84911006242     PISSN: 00217557     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jped.2014.05.003     Document Type: Short Survey

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