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Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2.
- Published in:
- Nature Genetics, 2000, v. 25, n. 4, p. 419, doi. 10.1038/78107
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- Publication type:
- Article
Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 387, doi. 10.1038/74224
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- Publication type:
- Article
A survey of TWIST for mutations in craniosynostosis reveals a variable length polyglycine tract in asymptomatic individuals.
- Published in:
- Human Mutation, 2001, v. 18, n. 6, p. 535, doi. 10.1002/humu.1230
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- Publication type:
- Article