Schmitt Gillenwater Kelly syndrome
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| Schmitt Gillenwater Kelly syndrome Classification and external resources |
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| OMIM | 179250 |
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Schmitt Gillenwater Kelly syndrome is an autosomal dominant syndrome consisting of radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillary diastema.
[edit] External links
- Schmitt E, Gillenwater JY, Kelly TE (1982). "An autosomal dominant syndrome of radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillary diastema". Am. J. Med. Genet. 13 (1): 63-9. doi:. PMID 7137222.
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