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Showing results (771-780 of 813) with videos related to

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American Journal of Human Genetics|July 25, 2017
Computational Prediction of Position Effects of Apparently Balanced Human Chromosomal RearrangementsCinthya J Zepeda-Mendoza, Jonas Ibn-Salem, Tammy Kammin, et al.
American Journal of Medical Genetics. Part A|June 18, 2019
Perinatal distress in 1p36 deletion syndrome can mimic hypoxic ischemic encephalopathyLauren B Carter, Agatino Battaglia, Athena Cherry, et al.
Leukemia|November 2, 2011
Hematopoietic cell transplantation for primary plasma cell leukemia: results from the Center for International Blood and Marrow Transplant ResearchA Mahindra, M E Kalaycio, J Vela-Ojeda, et al.
Diabetes, Obesity & Metabolism|May 31, 2017
Effects of MetAP2 inhibition on hyperphagia and body weight in Prader-Willi syndrome: A randomized, double-blind, placebo-controlled trialShawn E McCandless, Jack A Yanovski, Jennifer Miller, et al.
Frontiers in Aging Neuroscience|March 6, 2015
Bone mineral density, adiposity, and cognitive functionsHamid R Sohrabi, Kristyn A Bates, Michael Weinborn, et al.
Pediatric Neurology|August 13, 2021
Evaluating Sleep Disturbances in Children With Rare Genetic Neurodevelopmental SyndromesOlivia J Veatch, Beth A Malow, Hye-Seung Lee, et al.
The Journal of Clinical Endocrinology and Metabolism|January 3, 2026
Diazoxide Choline Extended-Release Tablets in Prader-Willi Syndrome: A Randomized, Double-Blind, Withdrawal Period StudyJennifer L Miller, Nicola Bridges, Eric I Felner, et al.
Communications Biology|February 25, 2021
Limited window for donation of convalescent plasma with high live-virus neutralizing antibody titers for COVID-19 immunotherapyAbhinay Gontu, Sreenidhi Srinivasan, Eric Salazar, et al.
The European Journal of Neuroscience|June 15, 2007
The phagocytic capacity of neuronesSamantha Bowen, Davidson D Ateh, Katrin Deinhardt, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 19, 2019
Rare SUZ12 variants commonly cause an overgrowth phenotypeSharri S Cyrus, Ana S A Cohen, Ruky Agbahovbe, et al.
Pageof 82

Showing results (771-780 of 813) with videos related to

Sort By:
Pageof 82
American Journal of Human Genetics|July 25, 2017
Computational Prediction of Position Effects of Apparently Balanced Human Chromosomal RearrangementsCinthya J Zepeda-Mendoza, Jonas Ibn-Salem, Tammy Kammin, et al.
American Journal of Medical Genetics. Part A|June 18, 2019
Perinatal distress in 1p36 deletion syndrome can mimic hypoxic ischemic encephalopathyLauren B Carter, Agatino Battaglia, Athena Cherry, et al.
Leukemia|November 2, 2011
Hematopoietic cell transplantation for primary plasma cell leukemia: results from the Center for International Blood and Marrow Transplant ResearchA Mahindra, M E Kalaycio, J Vela-Ojeda, et al.
Diabetes, Obesity & Metabolism|May 31, 2017
Effects of MetAP2 inhibition on hyperphagia and body weight in Prader-Willi syndrome: A randomized, double-blind, placebo-controlled trialShawn E McCandless, Jack A Yanovski, Jennifer Miller, et al.
Frontiers in Aging Neuroscience|March 6, 2015
Bone mineral density, adiposity, and cognitive functionsHamid R Sohrabi, Kristyn A Bates, Michael Weinborn, et al.
Pediatric Neurology|August 13, 2021
Evaluating Sleep Disturbances in Children With Rare Genetic Neurodevelopmental SyndromesOlivia J Veatch, Beth A Malow, Hye-Seung Lee, et al.
The Journal of Clinical Endocrinology and Metabolism|January 3, 2026
Diazoxide Choline Extended-Release Tablets in Prader-Willi Syndrome: A Randomized, Double-Blind, Withdrawal Period StudyJennifer L Miller, Nicola Bridges, Eric I Felner, et al.
Communications Biology|February 25, 2021
Limited window for donation of convalescent plasma with high live-virus neutralizing antibody titers for COVID-19 immunotherapyAbhinay Gontu, Sreenidhi Srinivasan, Eric Salazar, et al.
The European Journal of Neuroscience|June 15, 2007
The phagocytic capacity of neuronesSamantha Bowen, Davidson D Ateh, Katrin Deinhardt, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 19, 2019
Rare SUZ12 variants commonly cause an overgrowth phenotypeSharri S Cyrus, Ana S A Cohen, Ruky Agbahovbe, et al.
Pageof 82