Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Athena Chou"'
Publikováno v:
International Journal of Developmental Neuroscience. 31:434-447
The mammalian central nervous system (CNS) undergoes significant expansion postnatally, producing astrocytes, oligodendrocytes and inhibitory neurons to modulate the activity of neural circuits. This is coincident in humans with the emergence of pedi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::029c5ceffce832d5933870d98d46d8fe
https://doi.org/10.1016/j.ijdevneu.2013.03.008
https://doi.org/10.1016/j.ijdevneu.2013.03.008
Autor:
Tracey Oh, Cornelius F. Boerkoel, Kenneth J. Poskitt, Michelle Demos, Laura Arbour, Athena Chou, Tanya N. Nelson, Nataliya Tyshchenko, Margot I. Van Allen, Jingyi Yin, Barbara McGillivray, Andreas Rump, Robin Friedlander, Christèle du Souich, Jane Hurlburt
Publikováno v:
American Journal of Medical Genetics Part A. :2469-2478
X-linked mental retardation (XLMR) affects 1-2/1,000 males and accounts for approximately 10% of all mental retardation (MR). We have ascertained a syndromic form of XLMR segregating within a five-generation family with seven affected males. Prominen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb4549cf30e7b370978acee35fde0006
https://doi.org/10.1002/ajmg.a.33071
https://doi.org/10.1002/ajmg.a.33071
Publikováno v:
Clinical Genetics. 76:214-218
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65b8f02ce56c3cc510192172806bbd12
https://doi.org/10.1111/j.1399-0004.2009.01206.x
https://doi.org/10.1111/j.1399-0004.2009.01206.x
Autor:
F. Lucy Raymond, Jacques L. Michaud, Gail E. Herman, Jozef Gecz, Marco A. Marra, Barbara McGillivray, David W. Stockton, Jane Hurlburt, Robert D. Steiner, Richard A. Moore, Richard I. Kelley, Michelle Demos, Andrea E. DeBarber, Christèle du Souich, Laura Arbour, Keith W. McLarren, Ryan D. Morin, Paula J. Waters, Tesa M. Severson, Jessica E. Paul, Diane Wu, Yongjun Zhao, Patrick S. Tarpey, Michael R. Stratton, David Cunningham, Steven J.M. Jones, Louise S. Merkens, Karl-Heinz Grzeschik, Debbie Shears, Charles E. Schwartz, Lisa E. Kratz, Athena Chou, Jianghong An, Guy A. Rouleau, Margot I. Van Allen, Jingyi Yin, Cornelius F. Boerkoel, Glenda Hendson, Raffaella Smith, Tanya N. Nelson
Publikováno v:
The American Journal of Human Genetics. (6):905-914
CK syndrome (CKS) is an X-linked recessive intellectual disability syndrome characterized by dysmorphism, cortical brain malformations, and an asthenic build. Through an X chromosome single-nucleotide variant scan in the first reported family, we ide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2072794ba73871eb065b73c49bdf8f94
Publikováno v:
International Journal of Developmental Neuroscience; Oct2013, Vol. 31 Issue 6, p434-447, 14p
Publikováno v:
Chemical Senses; Mar2013, Vol. 38 Issue 3, p259-279, 21p
Publikováno v:
International Journal of Developmental Neuroscience; Jun2013, Vol. 31 Issue 4, pI-I, 1p