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American Journal of Human Genetics|September 14, 2001
Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35L J Hocking, C A Herbert, R K Nicholls, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 5, 2020
Cell-free DNA as a diagnostic analyte for molecular diagnosis of vascular malformationsKaitlyn Zenner, Dana M Jensen, Tori T Cook, et al.
The Canadian Journal of Cardiology|May 19, 2021
Cardiac Implantable Devices Management in Medical Assistance in Dying (MAiD): Review and Recommendations for Cardiac Device ClinicsSantabhanu Chakrabarti, Jennifer A Gibson, Matthew T Bennett, et al.
Lancet (London, England)|April 5, 1997
Linkage and association of insulin gene VNTR regulatory polymorphism with polycystic ovary syndromeD M Waterworth, S T Bennett, N Gharani, et al.
American Journal of Medical Genetics. Part A|June 7, 2016
A novel rasopathy caused by recurrent de novo missense mutations in PPP1CB closely resembles Noonan syndrome with loose anagen hairKaren W Gripp, Kimberly A Aldinger, James T Bennett, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|May 17, 2014
Effect of beta-blockers on QT dynamics in the long QT syndrome: measuring the benefitMatthew T Bennett, Lorne J Gula, George J Klein, et al.
Brain Research|May 26, 2015
Clinical indicators of paraplegia underplay universal spinal cord neuronal injury from transient aortic occlusionMarshall T Bell, Ferenc Puskas, Daine T Bennett, et al.
American Journal of Hematology|August 4, 2011
Improved differential diagnosis of anemia of chronic disease and iron deficiency anemia: a prospective multicenter evaluation of soluble transferrin receptor and the sTfR/log ferritin indexBarry S Skikne, Kari Punnonen, Paul H Caldron, et al.
American Journal of Medical Genetics. Part A|December 9, 2020
CHRNB1-associated congenital myasthenia syndrome: Expanding the clinical spectrumAmanda S Freed, Anisha C Schwarz, Brianna K Brei, et al.
JCI Insight|September 20, 2019
Genotype correlates with clinical severity in PIK3CA-associated lymphatic malformationsKaitlyn Zenner, Chi Vicky Cheng, Dana M Jensen, et al.
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