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Human Mutation|October 3, 2000
Characterization of two unusual RS1 gene deletions segregating in Danish retinoschisis familiesL Huopaniemi, H Tyynismaa, A Rantala, et al.Human Genetics|January 1, 1997
Refinement of the dominant optic atrophy locus (OPA1) to a 1.4-cM interval on chromosome 3q28-3q29, within a 3-Mb YAC contigA Jonasdottir, H Eiberg, B Kjer, et al.Archives Francaises De Pediatrie|May 1, 1976
[Salt-losing syndrome in newborn infants with hyperaldosteronism. Presenting a sensitivity to mineralocorticoids. Pseudohypoaldosteronism]M Tieder, E Vure, Y Gulboa, et al.Journal of Medical Genetics|September 1, 2010
Mutations in PCDH21 cause autosomal recessive cone-rod dystrophyE Ostergaard, M Batbayli, M Duno, et al.Rhinology|March 26, 2019
Does severe bleeding in HHT patients respond to intravenous bevacizumab? Review of the literature and case seriesT Rosenberg, A D Fialla, J Kjeldsen, et al.The British Journal of Ophthalmology|August 2, 2008
A novel founder BBS1 mutation explains a unique high prevalence of Bardet-Biedl syndrome in the Faroe IslandsT Duelund Hjortshøj, K Grønskov, K Brøndum-Nielsen, et al.International Journal of Clinical Practice|November 13, 2010
Biology and natural history of prostate cancer and the role of chemopreventionM T Rosenberg, M Froehner, D Albala, et al.The Canadian Journal of Urology|July 1, 2014
A practical primary care approach to lower urinary tract symptoms caused by benign prostatic hyperplasia (BPH-LUTS)Matt T Rosenberg, Erik S Witt, Martin Miner, et al.International Journal of Clinical Practice|July 14, 2020
Taking OAB seriously: A qualitative evaluation of primary care education on overactive bladder syndrome managementWendy Turell, Alexandra Howson, Scott A MacDiarmid, et al.Cancer|December 1, 1988
Flow cytometric analysis of breast needle aspiratesJ O Palmer, R W McDivitt, K R Stone, et al.Pageof 30