Waardenburg syndrome type I in a child with deletion (2) (q35q36.2)
- 15 November 1992
- journal article
- letter
- Published by Wiley in American Journal of Medical Genetics
- Vol. 44 (5) , 699-700
- https://doi.org/10.1002/ajmg.1320440533
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndromeNature, 1992
- Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box geneNature, 1992
- Waardenburg syndrome associated with meningomyeloceleAmerican Journal of Medical Genetics, 1992
- Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism.Proceedings of the National Academy of Sciences, 1991
- Mouse and hamster mutants as models for Waardenburg syndromes in humans.Journal of Medical Genetics, 1990
- Waardenburg syndrome type I in a child with de novo inversion (2)(q35q37.3)American Journal of Medical Genetics, 1989