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Kumarie Latchman

Showing results (1-10 of 5) with videos related to

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Mitochondrion|August 26, 2023
Mitochondrial dysfunction characterized in human induced pluripotent stem cell disease models in MELAS syndrome: A brief summaryKumarie Latchman, Mario Saporta, Carlos T Moraes
Journal of Pediatric Genetics|April 29, 2020
Spastic Diplegia in a Haitian Girl with Angelman SyndromeKumarie Latchman, Margarita Nieto-Moreno, Roberto Lopez Alberola
American Journal of Medical Genetics. Part A|December 14, 2019
Autosomal dominant inheritance in a recently described ZMIZ1-related neurodevelopmental disorder: Case report of siblings and an affected parentKumarie Latchman, Madison Calder, Dayna Morel, et al.
American Journal of Medical Genetics. Part A|January 7, 2022
Bilateral choanal stenosis in auriculocondylar syndrome caused by a PLCB4 variantLé Shon Peart, Joanna Gonzalez, Stephanie Bivona, et al.
Journal of Inherited Metabolic Disease|August 5, 2020
A founder noncoding GALT variant interfering with splicing causes galactosemiaKumarie Latchman, Jeanette Brown, Claire J Sineni, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Mitochondrion|August 26, 2023
Mitochondrial dysfunction characterized in human induced pluripotent stem cell disease models in MELAS syndrome: A brief summaryKumarie Latchman, Mario Saporta, Carlos T Moraes
Journal of Pediatric Genetics|April 29, 2020
Spastic Diplegia in a Haitian Girl with Angelman SyndromeKumarie Latchman, Margarita Nieto-Moreno, Roberto Lopez Alberola
American Journal of Medical Genetics. Part A|December 14, 2019
Autosomal dominant inheritance in a recently described ZMIZ1-related neurodevelopmental disorder: Case report of siblings and an affected parentKumarie Latchman, Madison Calder, Dayna Morel, et al.
American Journal of Medical Genetics. Part A|January 7, 2022
Bilateral choanal stenosis in auriculocondylar syndrome caused by a PLCB4 variantLé Shon Peart, Joanna Gonzalez, Stephanie Bivona, et al.
Journal of Inherited Metabolic Disease|August 5, 2020
A founder noncoding GALT variant interfering with splicing causes galactosemiaKumarie Latchman, Jeanette Brown, Claire J Sineni, et al.
Pageof 1