Analysis of the 5′ region of the caninePAX3gene and exclusion as a candidate for Dalmatian deafness1

Author:

Brenig B.,Pfeiffer I.,Jaggy A.,Kathmann I.,Balzari M.,Gaillard C.,Dolf G.

Publisher

Wiley

Subject

Genetics,Animal Science and Zoology,General Medicine

Reference25 articles.

1. Waardenburg syndrome (WS): the analysis of a single family with a WSI mutation showing linkage to RFLP markers on human chromosome 2q;Asher;American Journal of Human Genetics,1991

2. An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome;Baldwin;Nature,1992

3. Conservation of a large protein domain in the segmentation gene paired and in functionally related genes of Drosophila;Bopp;Cell,1986

4. Conservation of the paired domain in metazoans and its structure in three isolated human genes;Burd;EMBO Journal,1989

5. Effects of mutations at the W locus (c-kit) on inner ear pigmentation and function in the mouse;Cable;Pigment Cell Research,1994

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