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Achondrogenesis type I. A familial subvariant?

The clinical, pathological, and radiological features of 2 male sibs with a severe and lethal form of micromelic dwarfism are desribed. The family also includes 2 normal sibs. The histological and radiological appearances suggested a diagnosis of achondrogenesis type I, but the markedly deficient os...

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Bibliografische gegevens
Hoofdauteurs: Lauder, I, Ellis, H A, Ashcroft, T, Burridge, A
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 1976
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1546042/
https://ncbi.nlm.nih.gov/pubmed/962365
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