Friedman Tb

The incidence of deafness is non-randomly distributed among families segregating for Waardenburg syndrome type 1 (WS1).

T. Friedman, L. G. Robbins, R. Morell, 1997, Journal of medical genetics.

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.

K. Arnos, L. Farrer, P. Beighton, 1992, American journal of human genetics.