Authors: Diehl, Scott R. Boehnke, Michael Erickson, Robert P. Ploughman, Lynn M. Seiler, Kathleen A. Lieberman, Janice L. Clarke, H. Bush Bruce, Melissa A. Schorry, Elizabeth K. Pericak-Vance, Margaret O'Connell, Peter Collins, Francis S.

Citation: R. Diehl, Scott et al., A refined genetic map of the region of chromosome 17 surrounding the von recklinghausen neurofibromatosis (NFI) gene, American journal of human genetics , 44(1), 1989, pp. 33-37

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: MacLean, Charles J. Ploughman, Lynn M. Diehl, Scott R. Kendler, Kenneth S.

Citation: J. Maclean, Charles et al., A new test for linkage in the presence of locus heterogeneity., American journal of human genetics , 50-II(6), 1992, pp. 1259-1266