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The New England Journal of Medicine|November 7, 2008
A functional genetic link between distinct developmental language disordersSonja C Vernes, Dianne F Newbury, Brett S Abrahams, et al.Journal of Endocrinological Investigation|March 17, 2022
Testosterone does not affect lower urinary tract symptoms while improving markers of prostatitis in men with benign prostatic hyperplasia: a randomized clinical trialG Rastrelli, S Cipriani, F Lotti, et al.Genomics|April 11, 2000
Characterization of a highly complex region in Xq13 and mapping of three isodicentric breakpoints associated with preleukemiaN McDonell, J Ramser, F Francis, et al.Human Molecular Genetics|July 3, 2003
Myotubularin-related 2 protein phosphatase and neurofilament light chain protein, both mutated in CMT neuropathies, interact in peripheral nerveStefano C Previtali, Barbara Zerega, Diane L Sherman, et al.Genomics|November 5, 1997
A sequence-ready physical map of a region of 12q24.1B Renault, A Hovnanian, S Bryce, et al.Archives of Neurology|November 14, 2007
Choreoacanthocytosis in a Mexican familyJosé L Ruiz-Sandoval, Víctor García-Navarro, Erwin Chiquete, et al.European Journal of Human Genetics : EJHG|December 4, 2008
A 15q13.3 microdeletion segregating with autismAlistair T Pagnamenta, Kirsty Wing, Elham Sadighi Akha, et al.Genomics|October 27, 1997
Novel genes mapping to the critical region of the 5q- syndromeJ Boultwood, C Fidler, P Soularue, et al.American Journal of Human Genetics|April 11, 2003
A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11Matthew N Ogdie, I Laurence Macphie, Sonia L Minassian, et al.Journal of Neurodevelopmental Disorders|June 17, 2016
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypesKerry A Pettigrew, Emily Frinton, Ron Nudel, et al.Pageof 59