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
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