Die erbliche Osteopsathyrose

Fuss, H.

doi:10.1007/bf02801031

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1939

1970

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Cited by 16 publications

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“…Bell (1928), Fuss (1935) and Hills and McLanahan (1937) believe this disease is inherited as an autosomal dominant. Seedorff (1949) after studying 55 sibships with 180 affected individuals constructed a scheme based on the theories that each component of the syndrome of osteogenesis imperfecta was the result of a separate gene and that three separate genes controlled the bone fragility, mutation in the three collectively being responsible for osteogenesis imperfecta congenita.…”

Section: Discussionmentioning

confidence: 99%

Osteogenesis Imperfecta Congenita in Dizygotic Twins

Zeitoun¹,

Ibrahim²,

Kassem³

1963

Archives of Disease in Childhood

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