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Weiyi Mu

Showing results (31-40 of 48) with videos related to

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American Journal of Medical Genetics. Part A|September 5, 2018
Pain and sleep quality in children with non-vascular Ehlers-Danlos syndromesMichael Muriello, Julia L Clemens, Weiyi Mu, et al.
PEC Innovation|May 22, 2023
Evaluation of an educational conference for persons affected by hereditary frontotemporal degeneration and amyotrophic lateral sclerosisLaynie Dratch, Weiyi Mu, Elisabeth McCarty Wood, et al.
Journal of Child Health Care : for Professionals Working with Children in the Hospital and Community|September 21, 2022
Agreement between parent-proxy and child self-report in pediatric hypermobile Ehlers-Danlos syndromeYou Wang, Julia L Clemens, Michael Muriello, et al.
American Journal of Medical Genetics. Part A|September 24, 2015
Genotype-phenotype correlation of congenital anomalies in multiple congenital anomalies hypotonia seizures syndrome (MCAHS1)/PIGN-related epilepsyLeah Fleming, Monica Lemmon, Natalie Beck, et al.
American Journal of Medical Genetics. Part A|February 1, 2019
Factors affecting quality of life in children and adolescents with hypermobile Ehlers-Danlos syndrome/hypermobility spectrum disordersWeiyi Mu, Michael Muriello, Julia L Clemens, et al.
American Journal of Medical Genetics. Part A|May 18, 2019
Expansion of the clinical spectrum associated with AARS2-related disordersSiddharth Srivastava, Ankur Butala, Sonal Mahida, et al.
Neurology|September 30, 2025
The Importance of Offering Genetic Counseling and Testing to All Persons Diagnosed With Frontotemporal Degeneration Spectrum DisordersLaynie Dratch, Kim Jenny, Kristiana Salmon, et al.
Neurology|July 18, 2025
The Importance of Offering Genetic Counseling and Testing to All Persons Diagnosed With Frontotemporal Degeneration Spectrum DisordersLaynie Dratch, Kim Jenny, Kristiana Salmon, et al.
Elife|June 4, 2017
Transcription factor <i>TFCP2L1</i> patterns cells in the mouse kidney collecting ductsMax Werth, Kai M Schmidt-Ott, Thomas Leete, et al.
Human Genetics|September 30, 2016
De novo missense variants in PPP1CB are associated with intellectual disability and congenital heart diseaseLijiang Ma, Yavuz Bayram, Heather M McLaughlin, et al.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics. Part A|September 5, 2018
Pain and sleep quality in children with non-vascular Ehlers-Danlos syndromesMichael Muriello, Julia L Clemens, Weiyi Mu, et al.
PEC Innovation|May 22, 2023
Evaluation of an educational conference for persons affected by hereditary frontotemporal degeneration and amyotrophic lateral sclerosisLaynie Dratch, Weiyi Mu, Elisabeth McCarty Wood, et al.
Journal of Child Health Care : for Professionals Working with Children in the Hospital and Community|September 21, 2022
Agreement between parent-proxy and child self-report in pediatric hypermobile Ehlers-Danlos syndromeYou Wang, Julia L Clemens, Michael Muriello, et al.
American Journal of Medical Genetics. Part A|September 24, 2015
Genotype-phenotype correlation of congenital anomalies in multiple congenital anomalies hypotonia seizures syndrome (MCAHS1)/PIGN-related epilepsyLeah Fleming, Monica Lemmon, Natalie Beck, et al.
American Journal of Medical Genetics. Part A|February 1, 2019
Factors affecting quality of life in children and adolescents with hypermobile Ehlers-Danlos syndrome/hypermobility spectrum disordersWeiyi Mu, Michael Muriello, Julia L Clemens, et al.
American Journal of Medical Genetics. Part A|May 18, 2019
Expansion of the clinical spectrum associated with AARS2-related disordersSiddharth Srivastava, Ankur Butala, Sonal Mahida, et al.
Neurology|September 30, 2025
The Importance of Offering Genetic Counseling and Testing to All Persons Diagnosed With Frontotemporal Degeneration Spectrum DisordersLaynie Dratch, Kim Jenny, Kristiana Salmon, et al.
Neurology|July 18, 2025
The Importance of Offering Genetic Counseling and Testing to All Persons Diagnosed With Frontotemporal Degeneration Spectrum DisordersLaynie Dratch, Kim Jenny, Kristiana Salmon, et al.
Elife|June 4, 2017
Transcription factor <i>TFCP2L1</i> patterns cells in the mouse kidney collecting ductsMax Werth, Kai M Schmidt-Ott, Thomas Leete, et al.
Human Genetics|September 30, 2016
De novo missense variants in PPP1CB are associated with intellectual disability and congenital heart diseaseLijiang Ma, Yavuz Bayram, Heather M McLaughlin, et al.
Pageof 5