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Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 2, p. 151, doi. 10.1038/sj.ejhg.5201526
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- Article
Parietal foramina with cleidocranial dysplasia is caused by mutation in MSX2.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 11, p. 892, doi. 10.1038/sj.ejhg.5201062
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- Publication type:
- Article
Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 17, doi. 10.1038/83703
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- Article