Confirmation of the Location of a Waardenburg Syndrome Type I Mutation on Human Chromosome 2q.
- 1 September 1991
- journal article
- Published by Wiley in Annals of the New York Academy of Sciences
- Vol. 630 (1) , 295-297
- https://doi.org/10.1111/j.1749-6632.1991.tb19611.x
Abstract
No abstract availableKeywords
This publication has 3 references indexed in Scilit:
- Mouse and hamster mutants as models for Waardenburg syndromes in humans.Journal of Medical Genetics, 1990
- Strategies for multilocus linkage analysis in humans.Proceedings of the National Academy of Sciences, 1984
- Waardenburg's syndrome: A syndrome of heterochromia of the irides, lateral displacement of the medial canthi and lacrimal puncta, congenital deafness, and other characteristic associated defectsThe Journal of Pediatrics, 1960