Authors: Sykes, Bryan Ogilvie, Donald Wordsworth, Paul Wallis, Gillian Mathew, Chris Beighton, Peter Nicholls, Alan Pope, F. Michael Thompson, Elizabeth Tsipouras, Petros Schwartz, Robin Jensson, Olafur Arnason, Alfred Borresen, Anne-Lise Heiberg, Arvid Frey, Daniel Steinmann, Beat

Citation: Sykes, Bryan et al., Consistent linkage of dominantly inherited osteogenesis imperfecta to the type I collagen loci: COLIAl and COLIA2, American journal of human genetics , 46-I(2), 1990, pp. 293-307

Authors: Sher, Carron Ramesar, Rajkumar Martell, Robert Learmonth, Ian Tsipouras, Petros Beighton, Peter

Citation: Sher, Carron et al., Mild spondyloepiphyseal dysplasia (Namaqualand type): genetic linkage to the type II collagen gene COL2A1., American journal of human genetics , 48-I(3), 1991, pp. 518-524

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