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Results: 2
Waardenburg syndrome (WS): the analysis of a single family with a WS1 mutation showing linkage to RFLP markers on human chromosome 2q.
Authors: Asher, James H. Morell, Robert Friedman, Thomas B.
Citation: H. Asher, James et al., Waardenburg syndrome (WS): the analysis of a single family with a WS1 mutation showing linkage to RFLP markers on human chromosome 2q., American journal of human genetics , 48-I(1), 1991, pp. 43-52
Waardenberg 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
Authors: Farrer, Lindsay A. Grundfast, Kenneth M Amos, Jean Arnos, Kathleen S. Asher, James H. Beighton, Peter Diehl, Scott R. Fex, Jörgen Foy, Carole Friedman, Thomas B. Greenberg, Jacquie Hoth, Christopher Marazita, Mary Milunsky, Aubrey Morell, Robert Nance, Walter Newton, Valerie Ramesar, Rajkumar San Agustin, Theresa B. Skare, James Stevens, Cathy A. Wagner, Ronald G. Wilcox,Edward R. Winship, Ingrid Read, Andrew P.
Citation: A. Farrer, Lindsay et al., Waardenberg 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, American journal of human genetics , 50-II(5), 1992, pp. 902-913
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