Large-scale copy number variants (CNVs): Distribution in normal subjects and FISH/real-time qPCR analysis

by Nolin Sarah L, Harvard Chansonette, Liu Xudong, Qiao Ying, Brown W Ted, Koochek Maryam, Holden Jeanette JA, Lewis ME Suzanne, Rajcan-Separovic Evica
Published 2007-06-01

<it>DRD2</it> and <it>PPP1R1B</it> (<it>DARPP-32</it>) polymorphisms independently confer increased risk for autism spectrum disorders and additively predict affected status in mal...

by Hettinger Joe A, Liu Xudong, Hudson Melissa L, Lee Alana, Cohen Ira L, Michaelis Ron C, Schwartz Charles E, Lewis Suzanne ME, Holden Jeanette JA
Published 2012-05-01

XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene

by MacMillan Andrée, Macgregor David, Holinski-Feder Elke, Mangelsdorf Marie, Finnis Merran, Cason A Lauren, Stepp Monica L, Holden Jeanette JA, Gecz Jozef, Stevenson Roger E, Schwartz Charles E
Published 2005-04-01

Submicroscopic deletions of 11q24-25 in individuals without Jacobsen syndrome: re-examination of the critical region by high-resolution array-CGH

by VanAllen Margot I, Costa Teresa, McLeod Ross, Dyack Sarah, Gibson William, Clarke Lorne, Chudley Albert E, Arbour Laura, Farrell Sandra A, McGillivray Barbara, Bernier Francois P, Liu Xudong, Harvard Chansonette, Qiao Ying, Tyson Christine, Yong Siu-li, Graham Gail E, MacLeod Patrick, Patel Millan S, Hurlburt Jane, Holden Jeanette JA, Lewis Suzanne ME, Rajcan-Separovic Evica
Published 2008-11-01