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American Journal of Human Genetics|October 1, 1991
Identification of novel rhodopsin mutations associated with retinitis pigmentosa by GC-clamped denaturing gradient gel electrophoresisV C Sheffield, G A Fishman, J S Beck, et al.
Genome Biology|September 7, 2020
COCOA: coordinate covariation analysis of epigenetic heterogeneityJohn T Lawson, Jason P Smith, Stefan Bekiranov, et al.
Bioinformatics (Oxford, England)|April 3, 2018
BART: a transcription factor prediction tool with query gene sets or epigenomic profilesZhenjia Wang, Mete Civelek, Clint L Miller, et al.
American Journal of Human Genetics|June 23, 1998
Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43R Parvari, E Hershkovitz, A Kanis, et al.
Human Molecular Genetics|February 2, 2011
Functional analysis of BBS3 A89V that results in non-syndromic retinal degenerationPamela R Pretorius, Mohammed A Aldahmesh, Fowzan S Alkuraya, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 1, 1992
Ocular findings associated with rhodopsin gene codon 17 and codon 182 transition mutations in dominant retinitis pigmentosaG A Fishman, E M Stone, V C Sheffield, et al.
Genomics|May 1, 1993
The sensitivity of single-strand conformation polymorphism analysis for the detection of single base substitutionsV C Sheffield, J S Beck, A E Kwitek, et al.
Journal of Immunological Methods|September 15, 1993
Analysis of hapten-carrier protein conjugates by nondenaturing gel electrophoresisC Kamps-Holtzapple, R J Carlin, C Sheffield, et al.
Circulation|November 15, 1995
Molecular analysis of nondisjunction in Down syndrome patients with and without atrioventricular septal defectsM M Zittergruen, J C Murray, R M Lauer, et al.
Psychiatric Genetics|December 14, 2011
Germline mosaic transmission of a novel duplication of PXDN and MYT1L to two male half-siblings with autismKacie J Meyer, Michael S Axelsen, Val C Sheffield, et al.
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