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American Journal of Medical Genetics|July 13, 2002
Evaluation of FOXP2 as an autism susceptibility geneThomas H Wassink, Joseph Piven, Veronica J Vieland, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 16, 2010
Recurrence risks for Bardet-Biedl syndrome: Implications of locus heterogeneityJulie C Sapp, Darryl Nishimura, Jennifer J Johnston, et al.
Molecular Psychiatry|April 21, 2004
Examination of AVPR1a as an autism susceptibility geneT H Wassink, J Piven, V J Vieland, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 19, 2010
BBS6, BBS10, and BBS12 form a complex with CCT/TRiC family chaperonins and mediate BBSome assemblySeongjin Seo, Lisa M Baye, Nathan P Schulz, et al.
Plos One|April 5, 2013
Ectopic expression of human BBS4 can rescue Bardet-Biedl syndrome phenotypes in Bbs4 null miceXitiz Chamling, Seongjin Seo, Kevin Bugge, et al.
Nature Genetics|April 1, 1996
Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organificationV C Sheffield, Z Kraiem, J C Beck, et al.
Nature Genetics|September 1, 1995
Night blindness in Sorsby's fundus dystrophy reversed by vitamin AS G Jacobson, A V Cideciyan, G Regunath, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 26, 2008
Cortical enlargement in autism is associated with a functional VNTR in the monoamine oxidase A geneLea K Davis, Heather C Hazlett, Amy L Librant, et al.
Biorxiv : the Preprint Server for Biology|January 30, 2023
Determinants of renin cell differentiation: a single cell epi-transcriptomics approachAlexandre G Martini, Jason P Smith, Silvia Medrano, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|December 22, 1999
Clinical characterization and linkage analysis of a family with congenital X-linked nystagmus and deuteranomalyM L Mellott, J Brown, J H Fingert, et al.
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