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Results: 2
Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part III: Bipolar Disorder
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
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
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
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