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
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