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Journal of Biomedical Informatics|January 18, 2015
CNV-ROC: A cost effective, computer-aided analytical performance evaluator of chromosomal microarraysCorey W Goodman, Heather J Major, William D Walls, et al.
Nucleic Acids Research|August 24, 2024
Methods for constructing and evaluating consensus genomic interval setsJulia Rymuza, Yuchen Sun, Guangtao Zheng, et al.
Plos Genetics|June 24, 2015
Regulation of Insulin Receptor Trafficking by Bardet Biedl Syndrome ProteinsRachel D Starks, Andreas M Beyer, Deng Fu Guo, et al.
Investigative Ophthalmology & Visual Science|November 24, 2011
TUDCA slows retinal degeneration in two different mouse models of retinitis pigmentosa and prevents obesity in Bardet-Biedl syndrome type 1 miceArlene V Drack, Alina V Dumitrescu, Sajag Bhattarai, et al.
JAMA|June 22, 1999
Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafnessG E Green, D A Scott, J M McDonald, et al.
The American Journal of Pathology|September 1, 1995
Microsatellite instability in adenocarcinoma of the prostateR B Terrell, A H Wille, J C Cheville, et al.
American Journal of Medical Genetics. Part A|January 18, 2005
Clinical evidence of decreased olfaction in Bardet-Biedl syndrome caused by a deletion in the BBS4 geneAlessandro Iannaccone, Kirk Mykytyn, Antonio M Persico, et al.
Investigative Ophthalmology & Visual Science|July 1, 1994
RDS gene mutations causing retinitis pigmentosa or macular degeneration lead to the same abnormality in photoreceptor functionC M Kemp, S G Jacobson, A V Cideciyan, et al.
Women'S Health Issues : Official Publication of the Jacobs Institute of Women'S Health|July 7, 2026
State Midwifery Full Practice Authority Policies and Midwife-Attended Births Among Rural and Urban U.S. ResidentsClara E Busse, Emily C Sheffield, Caitlin Carroll, et al.
American Journal of Human Genetics|December 1, 1999
Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndromeL Ying, Y Katz, M Schlesinger, et al.
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