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Y Jane Tavyev

Showing results (1-10 of 7) with videos related to

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European Journal of Medical Genetics|May 3, 2012
Molecular bases and clinical spectrum of early infantile epileptic encephalopathiesY Jane Tavyev Asher, Fernando Scaglia
American Journal of Medical Genetics. Part A|April 29, 2010
The MECP2 duplication syndromeMelissa B Ramocki, Y Jane Tavyev, Sarika U Peters
European Journal of Medical Genetics|February 21, 2012
Clinical review of genetic epileptic encephalopathiesGrace J Noh, Y Jane Tavyev Asher, John M Graham
European Journal of Medical Genetics|February 28, 2012
De novo microdeletion of Xp11.3 exclusively encompassing the monoamine oxidase A and B genes in a male infant with episodic hypotonia: a genomics approach to personalized medicineRyan E O'Leary, Jean C Shih, Keith Hyland, et al.
Annals of Neurology|December 26, 2009
Autism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndromeMelissa B Ramocki, Sarika U Peters, Y Jane Tavyev, et al.
Human Molecular Genetics|March 28, 2009
Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switchingClaudia M B Carvalho, Feng Zhang, Pengfei Liu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 15, 2019
Diagnostic utility of transcriptome sequencing for rare Mendelian diseasesHane Lee, Alden Y Huang, Lee-Kai Wang, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
European Journal of Medical Genetics|May 3, 2012
Molecular bases and clinical spectrum of early infantile epileptic encephalopathiesY Jane Tavyev Asher, Fernando Scaglia
American Journal of Medical Genetics. Part A|April 29, 2010
The MECP2 duplication syndromeMelissa B Ramocki, Y Jane Tavyev, Sarika U Peters
European Journal of Medical Genetics|February 21, 2012
Clinical review of genetic epileptic encephalopathiesGrace J Noh, Y Jane Tavyev Asher, John M Graham
European Journal of Medical Genetics|February 28, 2012
De novo microdeletion of Xp11.3 exclusively encompassing the monoamine oxidase A and B genes in a male infant with episodic hypotonia: a genomics approach to personalized medicineRyan E O'Leary, Jean C Shih, Keith Hyland, et al.
Annals of Neurology|December 26, 2009
Autism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndromeMelissa B Ramocki, Sarika U Peters, Y Jane Tavyev, et al.
Human Molecular Genetics|March 28, 2009
Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switchingClaudia M B Carvalho, Feng Zhang, Pengfei Liu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 15, 2019
Diagnostic utility of transcriptome sequencing for rare Mendelian diseasesHane Lee, Alden Y Huang, Lee-Kai Wang, et al.
Pageof 1