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An Autosomal Recessive Form of Craniofacial Dysostosis (The Crouzon Syndrome)
Craniofacial dysostosis, the Crouzon syndrome, occurs sporadically and in families; the clearly heritable form up to now has been autosomal dominant. We ascertained two similarly affected sibs, a brother and a sister, in a sibship of nine. Neither the Negro parents nor any ancestors nor collateral r...
Sparad:
| Huvudupphovsmän: | , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
1973
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1012982/ https://ncbi.nlm.nih.gov/pubmed/4697859 |
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