A new variant of spondylometaphyseal dysplasia with autosomal dominant mode of inheritance.

Clinical and radiographic evaluation of an infant boy and his father revealed findings suggesting a new variant of spondylometaphyseal dysplasia with an apparently autosomal dominant mode of inheritance. The main clinical findings included short stature and marked ligamentous laxity in the infant. X...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: García-Castro, J M, Isales-Forsythe, C M, Díaz de Garau, P
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1982
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1048838/
https://ncbi.nlm.nih.gov/pubmed/7077620
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