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Results: 2
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
Assignment of the locus for waardenburg syndrome type I to human chromosome 2q37 and possible homology to the splotch mouse
Authors: Foy, Carole Newton, Valerie Wellesley, Diana Harris, Rodney Read, Andrew P.
Citation: Foy, Carole et al., Assignment of the locus for waardenburg syndrome type I to human chromosome 2q37 and possible homology to the splotch mouse, American journal of human genetics , 46-II(6), 1990, pp. 1017-1023
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