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D Cogan

Showing results (51-60 of 103) with videos related to

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American Journal of Ophthalmology|August 8, 2025
The Undiagnosed Diseases Network (UDN) Solves Ocular Syndromic Diagnostic DilemmasRory J Tinker, Logan M Smith, Lisa A Bastarache, 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.
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 Respiratory and Critical Care Medicine|August 29, 2022
Peripheral Blood Telomere Attrition in Persons at Risk for Familial Pulmonary FibrosisMargaret L Salisbury, Cheryl R Markin, Pingsheng Wu, 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.
American Journal of Respiratory and Critical Care Medicine|April 18, 2017
Rare Genetic Variants in PARN Are Associated with Pulmonary Fibrosis in FamiliesJonathan A Kropski, Sara Reiss, Cheryl Markin, et al.
The European Respiratory Journal|April 10, 2009
Alterations in oestrogen metabolism: implications for higher penetrance of familial pulmonary arterial hypertension in femalesE D Austin, J D Cogan, J D West, et al.
Clinical Endocrinology|December 18, 2003
Analysis of the PROP1 gene in a large cohort of patients with idiopathic hypogonadotropic hypogonadismJohn K Park, Metin Ozata, Lynn P Chorich, et al.
Pageof 11

Showing results (51-60 of 103) with videos related to

Sort By:
Pageof 11
American Journal of Ophthalmology|August 8, 2025
The Undiagnosed Diseases Network (UDN) Solves Ocular Syndromic Diagnostic DilemmasRory J Tinker, Logan M Smith, Lisa A Bastarache, 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.
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 Respiratory and Critical Care Medicine|August 29, 2022
Peripheral Blood Telomere Attrition in Persons at Risk for Familial Pulmonary FibrosisMargaret L Salisbury, Cheryl R Markin, Pingsheng Wu, 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.
American Journal of Respiratory and Critical Care Medicine|April 18, 2017
Rare Genetic Variants in PARN Are Associated with Pulmonary Fibrosis in FamiliesJonathan A Kropski, Sara Reiss, Cheryl Markin, et al.
The European Respiratory Journal|April 10, 2009
Alterations in oestrogen metabolism: implications for higher penetrance of familial pulmonary arterial hypertension in femalesE D Austin, J D Cogan, J D West, et al.
Clinical Endocrinology|December 18, 2003
Analysis of the PROP1 gene in a large cohort of patients with idiopathic hypogonadotropic hypogonadismJohn K Park, Metin Ozata, Lynn P Chorich, et al.
Pageof 11