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American Journal of Human Genetics|February 17, 2001
Linkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndromeR Caraballo, S Pavek, A Lemainque, et al.
Genes, Brain, and Behavior|March 30, 2010
A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31-q14.3L Addis, A D Friederici, S A Kotz, et al.
Transplantation|September 11, 2009
Outcomes with conversion from calcineurin inhibitors to sirolimus after renal transplantation in the context of steroid withdrawal or steroid continuationOgo I Egbuna, Roger B Davis, Robyn Chudinski, et al.
American Journal of Physiology. Endocrinology and Metabolism|June 23, 2016
Changes in the expression of the type 2 diabetes-associated gene VPS13C in the β-cell are associated with glucose intolerance in humans and miceZenobia B Mehta, Nicholas Fine, Timothy J Pullen, et al.
European Journal of Human Genetics : EJHG|May 6, 2010
Linkage and candidate gene studies of autism spectrum disorders in European populationsRichard Holt, Gabrielle Barnby, Elena Maestrini, et al.
Molecular Psychiatry|September 30, 2003
Analysis of reelin as a candidate gene for autismE Bonora, K S Beyer, J A Lamb, et al.
Somatic Cell and Molecular Genetics|November 1, 1987
Regional localization of the murine Duchenne muscular dystrophy gene on the mouse X chromosomeJ S Chamberlain, S G Grant, A A Reeves, et al.
Transplantation|March 25, 2008
SV40 infection associated with rituximab treatment after kidney transplantation in nonhuman primatesTakashi Maki, Angela Carville, Isaac E Stillman, et al.
Human Molecular Genetics|February 25, 2016
The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcriptsRobert Shore, Laura Covill, Kerry A Pettigrew, et al.
Genomics|July 24, 1998
Construction and characterization of a 10-fold genome equivalent rat P1-derived artificial chromosome libraryP Y Woon, K Osoegawa, P J Kaisaki, et al.
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