splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3

Author:

Epstein Douglas J.,Vekemans Michel,Gros Philippe

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference47 articles.

1. Current status of the ABO-Waardenburg syndrome type 1 linkage;Arias;Cytogenet. Cell Genet,1978

2. Mouse and hamster mutants as models for Waardenburg syndromes in humans;Asher;J. Med. Genet.,1990

3. Waardenburg syndrome (WS): the analysis of a single family with a WSI mutation showing linkage to RFLP markers on human chromosome 2q;Asher;Am. J. Hum. Genet.,1991

4. Analysis of the developmental effects of a lethal mutation in the house mouse;Auerbach;J. Exp. Zool.,1954

5. Undulated, a mutation affecting the development of the mouse skeleton, has a point mutation in the paired box of Pax 1;Balling;Cell,1988

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