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Human Molecular Genetics, Vol. 13, Iss. 16, 2004-08 ,pp. : 1775-1784

Oxford University Press

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Cutis laxa and excessive bone growth due to de novo mutations in PTDSS1

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John Wiley & Sons Inc

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Linkage disequilibrium between polymorphisms in the human TNFRSF1B gene and their association with bone mass in perimenopausal women

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Cardiopulmonary dysfunction in the Osteogenesis imperfecta mouse model Aga2 and human patients are caused by bone-independent mechanisms

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Defective bone mineralization and osteopenia in young adult FGFR3 −/− mice

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