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American Journal of Medical Genetics|September 1, 1990
Characterization of deletions in the dystrophin gene giving mild phenotypesD R Love, T J Flint, R F Marsden, et al.
Nature|January 11, 1990
Very mild muscular dystrophy associated with the deletion of 46% of dystrophinS B England, L V Nicholson, M A Johnson, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|July 24, 2004
Progesterone receptor by immunohistochemistry and clinical outcome in breast cancer: a validation studySyed K Mohsin, Heidi Weiss, Thomas Havighurst, et al.
JIMD Reports|November 22, 2017
Compound Heterozygous Inheritance of Mutations in Coenzyme Q8A Results in Autosomal Recessive Cerebellar Ataxia and Coenzyme Q<sub>10</sub> Deficiency in a Female Sib-PairJessie C Jacobsen, Whitney Whitford, Brendan Swan, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 15, 1991
Tissue distribution of the dystrophin-related gene product and expression in the mdx and dy mouseD R Love, G E Morris, J M Ellis, et al.
BMC Nephrology|April 22, 2024
A loss-of-function AGTR1 variant in a critically-ill infant with renal tubular dysgenesis: case presentation and literature reviewAljazi Al-Maraghi, Waleed Aamer, Mubarak Ziab, et al.
BMC Genomics|August 7, 2016
Comparative genomics and transcriptomics of Pichia pastorisKerry R Love, Kartik A Shah, Charles A Whittaker, et al.
Genomics|May 1, 1991
Sequences of junction fragments in the deletion-prone region of the dystrophin geneD R Love, S B England, A Speer, et al.
Heart Rhythm|February 20, 2010
Posthumous diagnosis of long QT syndrome from neonatal screening cardsP A Gladding, C-A Evans, J Crawford, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 8, 2011
Cytoplasmic estrogen receptor in breast cancerAllison W Welsh, Donald R Lannin, Gregory S Young, et al.
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