Normal hearing in Splotch (Sp/+), the mouse homologue of Waardenburg syndrome type 1

Author:

Steel Karen P.,Smith Richard J.H.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Reference40 articles.

1. Newton, V. Hearing loss and Waardenburg's syndrome: Implications for genetic counselling. J. Laryng. Otol. 104, 97–103 (1990).

2. Hageman, M.J. & Delleman, J W Heterogeneity in Waardenburg syndrome. Am. J. hum. Genet. 29, 468–485 (1977).

3. Farrer, L.A., et al. Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: First report of the WS Consortium. Am. J. hum. Genet. 50, 902–913 (1992).

4. Asher, J.H. & Friedman, T.B. Mouse and hamster mutants as models for Waardenburg syndromes in humans. J. med. Genet. 27, 618–626. (1990).

5. Foy, C., Newton, V., Wellesley, D., Harris, R. & Read, A.P. Assignment of the locus for Waardenburg syndrome type 1 to human chromosome 2q37 and possible homology to the Splotch mouse. Am. J. hum. Genet. 46, 1017–1023 (1990).

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