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Annals of Internal Medicine|January 1, 1985
Evidence for active Epstein-Barr virus infection in patients with persistent, unexplained illnesses: elevated anti-early antigen antibodiesJ F Jones, C G Ray, L L Minnich, et al.
The Journal of Clinical Endocrinology and Metabolism|September 24, 1998
The PROP1 2-base pair deletion is a common cause of combined pituitary hormone deficiencyJ D Cogan, W Wu, J A Phillips, et al.
Archives of Pathology & Laboratory Medicine|October 1, 1983
Age-related changes in T- and B-lymphocyte subpopulations in the peripheral bloodM J Hicks, J F Jones, L L Minnich, et al.
JAMA|October 2, 1981
In utero Epstein-Barr virus (infectious mononucleosis) infectionG N Goldberg, V A Fulginiti, C G Ray, et al.
Population Health Metrics|March 15, 2016
Methods of applying the 1994 case definition of chronic fatigue syndrome - impact on classification and observed illness characteristicsE R Unger, J-M S Lin, H Tian, et al.
Lancet (London, England)|July 18, 1981
Treatment of childhood combined Epstein-Barr virus/cytomegalovirus infection with oral bovine transfer factorJ F Jones, L L Minnich, W S Jeter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 19, 2005
Gross BMPR2 gene rearrangements constitute a new cause for primary pulmonary hypertensionJoy D Cogan, Cindy L Vnencak-Jones, John A Phillips, et al.
American Journal of Medical Genetics. Part A|April 27, 2026
Diagnostic Odyssey of Atypical Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (LCHADD) Explained by Three Allelic Products From Two Pathogenic VariantsYutaka Furuta, Lynette C Rives, T Andrew Burrow, et al.
American Journal of Medical Genetics. Part A|October 28, 2023
Probable digenic inheritance of Diamond-Blackfan anemiaYutaka Furuta, Rory J Tinker, Alican Gulsevin, et al.
American Journal of Medical Genetics. Part A|March 21, 2024
Undiagnosed Disease Network collaborative approach in diagnosing rare disease in a patient with a mosaic CACNA1D variantKimberly M Ezell, Rory J Tinker, Yutaka Furuta, et al.
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