Authors: Dick, Danielle M. Foroud, Tatiana Flury, Leah Bowman, Elizabeth S. Miller, Marvin J. Rau, N. Leela Moe, P. Ryan Samavedy, Nalini El-Mallakh, Rif Manji, Husseini Glitz, Debra A. Meyer, Eric T. Smiley, Carrie Hahn, Rhoda Widmark, Clifford McKinney, Rebecca Sutton, Laura Ballas, Christos Grice, Dorothy Berrettini, Wade Byerley, William Coryell, William DePaulo, Raymond MacKinnon, Dean F. Gershon, Elliot S. Kelsoe, John R. McMahon, Francis J. McInnis, Melvin Murphy, Dennis L. Reich, Theodore Scheftner, William Nurnberger, John I. , Jr.

Citation: M. Dick, Danielle et al., Genomewide Linkage Analyses of Bipolar Disorder: A New Sample of 250 Pedigrees from the National Institute of Mental Health Genetics Initiative, American journal of human genetics , 73(1), 2003, pp. 107-114

Authors: Lin, Ping-I McInnis, Melvin G. Potash, James B. Willour, Virginia L. MacKinnon, Dean F. Miao, Kuangyi DePaulo, Raymond J. Zandi, Peter P.

Citation: Lin, Ping-i et al., Léri-Weill dyschondrosteosis (LWD) is a pseudoautosomal dominant disorder characterized by disproportionate short stature and a characteristic curving of the radius, known as the .Madelung deformity..SHOX mutations resulting in SHOX haploinsufficiency have been found in LWD and in a variable proportion of patients with idiopathic short stature (ISS), whereas homozygous loss of SHOX results in the more severe Langer mesomelic dysplasia (LMD). Defects in SHOX have been identified in .60% of LWD ca, American journal of human genetics , 77(4), 2005, pp. 545-555