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Journal of Neurodevelopmental Disorders|January 18, 2014
Associations of HLA alleles with specific language impairmentRon Nudel, Nuala H Simpson, Gillian Baird, et al.
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.
Transplantation|April 29, 2004
Subclinical rejection and borderline changes in early protocol biopsy specimens after renal transplantationIan S D Roberts, Srikanth Reddy, Christine Russell, et al.
Transplant International : Official Journal of the European Society for Organ Transplantation|September 7, 2004
The impact of thiopurine S-methyltransferase polymorphisms on azathioprine dose 1 year after renal transplantationMargarete A Fabre, Des C Jones, Mike Bunce, 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.
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.
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.
Autism Research : Official Journal of the International Society for Autism Research|March 18, 2014
A deletion involving CD38 and BST1 results in a fusion transcript in a patient with autism and asthmaFabiola Ceroni, Angela Sagar, Nuala H Simpson, et al.
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