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Journal of the American Society of Nephrology : JASN|May 13, 2005
On the intraoperative molecular status of renal allografts after vascular reperfusion and clinical outcomesYingyos Avihingsanon, Naili Ma, Martha Pavlakis, et al.Cancer Genetics and Cytogenetics|December 1, 1993
Identification of a yeast artificial chromosome that spans the human papillary renal cell carcinoma-associated t(X;1) breakpoint in Xp11.2R F Suijkerbuijk, A M Meloni, R J Sinke, et al.Human Molecular Genetics|July 1, 1994
X-linked mixed deafness (DFN3): cloning and characterization of the critical region allows the identification of novel microdeletionsI Huber, M Bitner-Glindzicz, Y J de Kok, et al.Brain Structure & Function|August 12, 2016
Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout miceIsabel Martinez-Garay, Luiz G Guidi, Zoe G Holloway, et al.Molecular Psychiatry|November 1, 2003
Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII geneE Bacchelli, F Blasi, M Biondolillo, et al.Molecular Psychiatry|November 20, 2003
Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effectsS K Loo, S E Fisher, C Francks, et al.American Journal of Human Genetics|May 7, 2005
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficitsKay D MacDermot, Elena Bonora, Nuala Sykes, et al.Journal of Neurodevelopmental Disorders|January 18, 2014
Associations of HLA alleles with specific language impairmentRon Nudel, Nuala H Simpson, Gillian Baird, et al.Plos One|November 10, 2010
Identification of candidate genes for dyslexia susceptibility on chromosome 18Thomas S Scerri, Silvia Paracchini, Andrew Morris, et al.American Journal of Human Genetics|July 6, 2000
The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorderC S Lai, S E Fisher, J A Hurst, et al.Pageof 59