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Grace Yoon

Showing results (41-50 of 177) with videos related to

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Neuromuscular Disorders : NMD|March 23, 2010
Cap myopathy caused by a mutation of the skeletal alpha-actin gene ACTA1Ryan M Hung, Grace Yoon, Cynthia E Hawkins, et al.
Muscle & Nerve|April 14, 2012
Milder phenotype of congenital muscular dystrophy in a novel POMT1 mutationSamiah A Al-Zaidy, Berivan Baskin, Cynthia Hawkins, et al.
Pediatric Nephrology (Berlin, Germany)|July 19, 2017
Neonatal stroke and haematuria: QuestionsSally Kellett, Mathieu Lemaire, Steven P Miller, et al.
Pediatric Nephrology (Berlin, Germany)|July 19, 2017
Neonatal stroke and haematuria: AnswersSally Kellett, Mathieu Lemaire, Steven P Miller, et al.
Medical and Pediatric Oncology|February 12, 2002
Neuroblastoma in a patient with the Beckwith-Wiedemann syndrome (BWS)Grace Yoon, Gail Graham, Rosanna Weksberg, et al.
Journal of Medical Genetics|January 23, 2025
Homozygous missense variant in <i>C2orf69</i> causes early-onset neurodegeneration, leukoencephalopathy and autoinflammationRachel Youjin Oh, Michael Maier, Susan Blaser, et al.
The Journal of Headache and Pain|December 20, 2005
Clinic-based study of family history of vascular risk factors and migraineGrace Yoon, Susan Baggaley, Peter Bacchetti, et al.
American Journal of Medical Genetics. Part A|October 6, 2017
Noncompaction cardiomyopathy in an infant with Walker-Warburg syndromeSarah Abdullah, Cynthia Hawkins, Gregory Wilson, et al.
Human Genetics|November 4, 2008
Ataxia and pancytopenia caused by a mutation in TINF2Elena Tsangaris, Sally-Lin Adams, Grace Yoon, et al.
Neuromuscular Disorders : NMD|December 28, 2010
Symptomatic dystrophinopathies in female childrenNatashia Seemann, Kathy Selby, Laura McAdam, et al.
Pageof 18

Showing results (41-50 of 177) with videos related to

Sort By:
Pageof 18
Neuromuscular Disorders : NMD|March 23, 2010
Cap myopathy caused by a mutation of the skeletal alpha-actin gene ACTA1Ryan M Hung, Grace Yoon, Cynthia E Hawkins, et al.
Muscle & Nerve|April 14, 2012
Milder phenotype of congenital muscular dystrophy in a novel POMT1 mutationSamiah A Al-Zaidy, Berivan Baskin, Cynthia Hawkins, et al.
Pediatric Nephrology (Berlin, Germany)|July 19, 2017
Neonatal stroke and haematuria: QuestionsSally Kellett, Mathieu Lemaire, Steven P Miller, et al.
Pediatric Nephrology (Berlin, Germany)|July 19, 2017
Neonatal stroke and haematuria: AnswersSally Kellett, Mathieu Lemaire, Steven P Miller, et al.
Medical and Pediatric Oncology|February 12, 2002
Neuroblastoma in a patient with the Beckwith-Wiedemann syndrome (BWS)Grace Yoon, Gail Graham, Rosanna Weksberg, et al.
Journal of Medical Genetics|January 23, 2025
Homozygous missense variant in <i>C2orf69</i> causes early-onset neurodegeneration, leukoencephalopathy and autoinflammationRachel Youjin Oh, Michael Maier, Susan Blaser, et al.
The Journal of Headache and Pain|December 20, 2005
Clinic-based study of family history of vascular risk factors and migraineGrace Yoon, Susan Baggaley, Peter Bacchetti, et al.
American Journal of Medical Genetics. Part A|October 6, 2017
Noncompaction cardiomyopathy in an infant with Walker-Warburg syndromeSarah Abdullah, Cynthia Hawkins, Gregory Wilson, et al.
Human Genetics|November 4, 2008
Ataxia and pancytopenia caused by a mutation in TINF2Elena Tsangaris, Sally-Lin Adams, Grace Yoon, et al.
Neuromuscular Disorders : NMD|December 28, 2010
Symptomatic dystrophinopathies in female childrenNatashia Seemann, Kathy Selby, Laura McAdam, et al.
Pageof 18