Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Holden, Jeanette JA"'
Autor:
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
Publikováno v:
Behavioral and Brain Functions, Vol 8, Iss 1, p 19 (2012)
Abstract Background The neurotransmitter dopamine (DA) modulates executive functions, learning, and emotional processing, all of which are impaired in individuals with autism spectrum disorders (ASDs). Our previous findings suggest a role for dopamin
Externí odkaz:
https://doaj.org/article/9a9d721ef95c471d8c399ba2926e0731
Autor:
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
Publikováno v:
Molecular Cytogenetics, Vol 1, Iss 1, p 23 (2008)
Abstract Background Jacobsen syndrome is a rare contiguous gene disorder that results from a terminal deletion of the long arm of chromosome 11. It is typically characterized by intellectual disability, a variety of physical anomalies and a distincti
Externí odkaz:
https://doaj.org/article/c6659ceb0ffb4bc898e369a05ef7a6bd
Autor:
Nolin Sarah L, Harvard Chansonette, Liu Xudong, Qiao Ying, Brown W Ted, Koochek Maryam, Holden Jeanette JA, Lewis ME Suzanne, Rajcan-Separovic Evica
Publikováno v:
BMC Genomics, Vol 8, Iss 1, p 167 (2007)
Abstract Background Genomic copy number variants (CNVs) involving >1 kb of DNA have recently been found to be widely distributed throughout the human genome. They represent a newly recognized form of DNA variation in normal populations, discovered th
Externí odkaz:
https://doaj.org/article/d41da948e40449b08bbeb2b8bdd0a900
Autor:
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
Publikováno v:
BMC Medical Genetics, Vol 6, Iss 1, p 16 (2005)
Abstract Background X-linked mental retardation (XLMR) is the leading cause of mental retardation in males. Mutations in the ARX gene in Xp22.1 have been found in numerous families with both nonsyndromic and syndromic XLMR. The most frequent mutation
Externí odkaz:
https://doaj.org/article/338cd399448d4c11b86065723c7421b5
Autor:
Liu, Xudong, Malenfant, Patrick, Reesor, Chelsea, Lee, Alana, Hudson, Melissa L, Harvard, Chansonette, Qiao, Ying, Persico, Antonio M, Cohen, Ira L, Chudley, Albert E, Forster-Gibson, Cynthia, Rajcan-Separovic, Evica, Lewis, ME Suzanne, Holden, Jeanette JA
Publikováno v:
European Journal of Human Genetics; Dec2011, Vol. 19 Issue 12, p1264-1270, 7p, 1 Diagram, 4 Charts
Autor:
Ying Qiao, Xudong Liu, Harvard, Chansonette, Nolin, Sarah L, Brown, W Ted, Koochek, Maryam, Holden, Jeanette JA, Lewis, ME Suzanne, Rajcan-Separovic, Evica
Publikováno v:
BMC Genomics; 2007, Vol. 8, p167-11, 11p, 4 Color Photographs, 3 Diagrams, 3 Charts
Autor:
Stepp, Monica L, Cason, A Lauren, Finnis, Merran, Mangelsdorf, Marie, Holinski-Feder, Elke, Macgregor, David, MacMillan, Andree, Holden, Jeanette JA, Gecz, Jozef, Stevenson, Roger E, Schwartz, Charles E
Publikováno v:
BMC Medical Genetics; 2005, Vol. 6, p16-4, 4p, 1 Graph
Autor:
Tyson C; Department of Pathology and Laboratory Medicine and Child and Family Research Institute (CFRI), UBC, Vancouver, BC, Canada. eseparovic@cw.bc.ca., Qiao Y, Harvard C, Liu X, Bernier FP, McGillivray B, Farrell SA, Arbour L, Chudley AE, Clarke L, Gibson W, Dyack S, McLeod R, Costa T, Vanallen MI, Yong SL, Graham GE, Macleod P, Patel MS, Hurlburt J, Holden JJ, Lewis SM, Rajcan-Separovic E
Publikováno v:
Molecular cytogenetics [Mol Cytogenet] 2008 Nov 11; Vol. 1, pp. 23. Date of Electronic Publication: 2008 Nov 11.