Classification of osteogenesis imperfecta.

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Osteogenesis imperfecta and clubfoot-a rare combination: Case report and review of the literature.Mutational analysis of COL1A1 and COL1A2 genes among Estonian osteogenesis imperfecta patients Bisphosphonate therapy and osteogenesis imperfecta: The lived experience of children and their mothers.

P2860

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P2860

Classification of osteogenesis imperfecta.

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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name

Classification of osteogenesis imperfecta.

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Classification of osteogenesis imperfecta.

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Classification of osteogenesis imperfecta.

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P1476

Classification of osteogenesis imperfecta

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P2093

Barbara M Misof

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Klaus Klaushofer

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Paul Roschger

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P2860

Genetic heterogeneity in osteogenesis imperfecta.

Mutations in SERPINF1 cause osteogenesis imperfecta type VI

Homozygosity for a missense mutation in SERPINH1, which encodes the collagen chaperone protein HSP47, results in severe recessive osteogenesis imperfecta

CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta

Syndromes with congenital brittle bones

Osteogenesis imperfecta due to mutations in non-collagenous genes: lessons in the biology of bone formation

Bone collagen: new clues to its mineralization mechanism from recessive osteogenesis imperfecta

New genes in bone development: what's new in osteogenesis imperfecta

Osteogenesis imperfecta: clinical diagnosis, nomenclature and severity assessment

CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta

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s10354-015-0368-3

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264-270

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scholarly article

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10.1007/S10354-015-0368-3

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13-14

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165

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N Fratzl-Zelman

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2015-07-25T00:00:00Z

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1038564404

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26208476

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P921

osteogenesis imperfecta

Classification of osteogenesis imperfecta.

about

P2860

P2860

Classification of osteogenesis imperfecta.

description

name

type

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P1433

P1476

P2093

P2860

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