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Grace Yoon

Showing results (21-30 of 177) with videos related to

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Annals of Medicine|June 5, 2004
Andersen-Tawil syndrome: a model of clinical variability, pleiotropy, and genetic heterogeneityMatthew R Donaldson, Grace Yoon, Ying-Hui Fu, et al.
The Journal of Pediatrics|April 7, 2005
Dizygotic twin pregnancy conceived with assisted reproductive technology associated with chromosomal anomaly, imprinting disorder, and monochorionic placentationGrace Yoon, Linda S Beischel, John P Johnson, et al.
Journal of Leukocyte Biology|May 17, 2024
The role of cathelicidins in neutrophil biologyGrace Yoon, Rodrigo Puentes, Jacquelyn Tran, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
Magnetic resonance imaging of a unique mutation in a family with Pelizaeus-Merzbacher diseaseElka Miller, Elysa Widjaja, Daniel Nilsson, et al.
Neurology|January 15, 2025
Child Neurology: Severe <i>GMPPB</i>-Related Congenital Muscular Dystrophy With Rapidly Progressive Encephalopathy Leading to Infantile DeathJoseph Dubé, Susan Blaser, Anne-Marie Guerguerian, et al.
Annals of Neurology|December 27, 2016
KCNA2 mutations are rare in hereditary spastic paraplegiaZiv Gan-Or, Grace Yoon, Oksana Suchowersky, et al.
AJNR. American Journal of Neuroradiology|May 30, 2024
Imaging Findings and MRI Patterns in a Cohort of 18q Chromosomal AbnormalitiesPrateek Malik, Helen Branson, Grace Yoon, et al.
American Journal of Medical Genetics. Part A|January 26, 2018
Response to phenotypic hetergeneity of POMT2 variantsAndrea Guerin, Gregory Wilson, Sarah Abdullah, et al.
European Journal of Human Genetics : EJHG|April 6, 2017
Severe neurodegeneration, progressive cerebral volume loss and diffuse hypomyelination associated with a homozygous frameshift mutation in CSTBAlan O'Brien, Christian R Marshall, Susan Blaser, et al.
Neurology|March 15, 2020
Pearls & Oy-sters: Fatal brain edema is a rare complication of severe CACNA1A-related disorderLaurence Gauquelin, Cynthia Hawkins, Emily W Y Tam, et al.
Pageof 18

Showing results (21-30 of 177) with videos related to

Sort By:
Pageof 18
Annals of Medicine|June 5, 2004
Andersen-Tawil syndrome: a model of clinical variability, pleiotropy, and genetic heterogeneityMatthew R Donaldson, Grace Yoon, Ying-Hui Fu, et al.
The Journal of Pediatrics|April 7, 2005
Dizygotic twin pregnancy conceived with assisted reproductive technology associated with chromosomal anomaly, imprinting disorder, and monochorionic placentationGrace Yoon, Linda S Beischel, John P Johnson, et al.
Journal of Leukocyte Biology|May 17, 2024
The role of cathelicidins in neutrophil biologyGrace Yoon, Rodrigo Puentes, Jacquelyn Tran, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
Magnetic resonance imaging of a unique mutation in a family with Pelizaeus-Merzbacher diseaseElka Miller, Elysa Widjaja, Daniel Nilsson, et al.
Neurology|January 15, 2025
Child Neurology: Severe <i>GMPPB</i>-Related Congenital Muscular Dystrophy With Rapidly Progressive Encephalopathy Leading to Infantile DeathJoseph Dubé, Susan Blaser, Anne-Marie Guerguerian, et al.
Annals of Neurology|December 27, 2016
KCNA2 mutations are rare in hereditary spastic paraplegiaZiv Gan-Or, Grace Yoon, Oksana Suchowersky, et al.
AJNR. American Journal of Neuroradiology|May 30, 2024
Imaging Findings and MRI Patterns in a Cohort of 18q Chromosomal AbnormalitiesPrateek Malik, Helen Branson, Grace Yoon, et al.
American Journal of Medical Genetics. Part A|January 26, 2018
Response to phenotypic hetergeneity of POMT2 variantsAndrea Guerin, Gregory Wilson, Sarah Abdullah, et al.
European Journal of Human Genetics : EJHG|April 6, 2017
Severe neurodegeneration, progressive cerebral volume loss and diffuse hypomyelination associated with a homozygous frameshift mutation in CSTBAlan O'Brien, Christian R Marshall, Susan Blaser, et al.
Neurology|March 15, 2020
Pearls & Oy-sters: Fatal brain edema is a rare complication of severe CACNA1A-related disorderLaurence Gauquelin, Cynthia Hawkins, Emily W Y Tam, et al.
Pageof 18