Authors:
Segurado, Ricardo
Detera-Wadleigh, Sevilla D.
Levinson, Douglas F.
Lewis, Cathryn M.
Gil, Michael
Nurnberger, John I., Jr.
Craddock, Nick
DePaulo, Raymond J.
Baron, Miron
Gershon, Elliot S.
Ekhoolm, Jenny
Cichon, Sven
Turecki, Gustavo
Claes, Stephan
Kelsoe, John R.
Badenhop, Renee F.
Morissette, J.
Coon, Hilary
Blackwood, Douglas
McInnes, L.Allison
Foroud, Tatiana
Edenberg, Howard J.
Reich, Theodore
Rice, John P.
Goate, Alison
McInnis, Melvin G.
McMahon, Francis J.
Badner, Judith A.
Goldin, Lynn R.
Bennett, Phil
Willour, Virginia L.
Zandi, Peter P.
Liu, Jianjun
Gillam, Conrad
Juo, Suh-Hang
Berrettini, Wade H.
Yoshikawa, Takeo
Peltonen, Leena
Lönnqvist, Juoko
Nöthen, Markus M.
Schumacher, Johannes
Windemuth, Christine
Rietschel, Marcella
Proppin, Peter
Maier, Wolfgang
Alda, Martin
Grof, Paul
Rouleau, Guy A.
Del-Favero, Jurgen
Van Broeckhoven, Christine
Mendlewicz, Julien
Adolfsson, Rolf
Spence, M. Anne
Luebbert, Hermann
Adams, Linda J.
Donald, Jennifer A.
Mitchell, Philip B.
Barden, Nicholas
Shink, Eric
Byerley, William
Muir, Walter
Visscher, Peter M.
Macgregor, Stuart
Gurling, Hugh
Kalsi, Gursharan
McQuillin, Andrew
Escamilla, Michael A.
Reus, Victor I.
Leon, Pedro
Freimer, Nelson B.
Ewald, Henrik
Kruse, Torben A.
Mors, Ole
Radhakrishna, Uppala
Blouin, Jean-Louis
Antonarakis, Stylianos
Akarsu, Nurten
Citation: Segurado, Ricardo et al., Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part III: Bipolar Disorder, American journal of human genetics , 73(1), 2003, pp. 49-62
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