Search research articles
Contact Us
Filters
Showing results (81-90 of 107) with videos related to
Page
of 11
Sort By:
Genes
|
August 29, 2024
Clinical Features and Disease Progression in Older Individuals with Rett Syndrome
Jeffrey L Neul, Timothy A Benke, Eric D Marsh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 13, 2016
Enrichment of mutations in chromatin regulators in people with Rett syndrome lacking mutations in MECP2
Samin A Sajan, Shalini N Jhangiani, Donna M Muzny, et al.
Annals of Neurology
|
May 9, 2024
Electroencephalographic Correlates of Clinical Severity in the Natural history study of RTT and Related Disorders
Joni N Saby, Patrick J Mulcahey, Timothy A Benke, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 8, 2025
Altered oscillatory coupling reflects possible inhibitory interneuron dysfunction in Rett syndrome
Devorah Kranz, Yael Braverman, Michelle McCarthy, et al.
Journal of Medical Genetics
|
January 9, 2014
Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome
Vishnu Anand Cuddapah, Rajesh B Pillai, Kiran V Shekar, et al.
American Journal of Medical Genetics. Part A
|
September 28, 2023
Parental age effects and Rett syndrome
Xiaolan Fang, Lauren M Baggett, Raymond C Caylor, et al.
The Journal of Pediatrics
|
January 22, 2022
Anthropometric Measures Correspond with Functional Motor Outcomes in Females with Rett Syndrome
Kathleen J Motil, Suzanne Geerts, Fran Annese, et al.
The Journal of Molecular Diagnostics : JMD
|
February 11, 2014
Development of a genomic DNA reference material panel for Rett syndrome (MECP2-related disorders) genetic testing
Lisa V Kalman, Jack C Tarleton, Alan K Percy, et al.
Journal of Neurodevelopmental Disorders
|
March 4, 2023
Comparison of evoked potentials across four related developmental encephalopathies
Joni N Saby, Sarika U Peters, Timothy A Benke, et al.
American Journal of Medical Genetics. Part A
|
November 10, 2020
Phenotypic features in MECP2 duplication syndrome: Effects of age
Sarika U Peters, Cary Fu, Eric D Marsh, et al.
Page
of 11
Search research articles
Search
Showing results (81-90 of 107) with videos related to
Sort By:
Page
of 11
Genes
|
August 29, 2024
Clinical Features and Disease Progression in Older Individuals with Rett Syndrome
Jeffrey L Neul, Timothy A Benke, Eric D Marsh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 13, 2016
Enrichment of mutations in chromatin regulators in people with Rett syndrome lacking mutations in MECP2
Samin A Sajan, Shalini N Jhangiani, Donna M Muzny, et al.
Annals of Neurology
|
May 9, 2024
Electroencephalographic Correlates of Clinical Severity in the Natural history study of RTT and Related Disorders
Joni N Saby, Patrick J Mulcahey, Timothy A Benke, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 8, 2025
Altered oscillatory coupling reflects possible inhibitory interneuron dysfunction in Rett syndrome
Devorah Kranz, Yael Braverman, Michelle McCarthy, et al.
Journal of Medical Genetics
|
January 9, 2014
Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome
Vishnu Anand Cuddapah, Rajesh B Pillai, Kiran V Shekar, et al.
American Journal of Medical Genetics. Part A
|
September 28, 2023
Parental age effects and Rett syndrome
Xiaolan Fang, Lauren M Baggett, Raymond C Caylor, et al.
The Journal of Pediatrics
|
January 22, 2022
Anthropometric Measures Correspond with Functional Motor Outcomes in Females with Rett Syndrome
Kathleen J Motil, Suzanne Geerts, Fran Annese, et al.
The Journal of Molecular Diagnostics : JMD
|
February 11, 2014
Development of a genomic DNA reference material panel for Rett syndrome (MECP2-related disorders) genetic testing
Lisa V Kalman, Jack C Tarleton, Alan K Percy, et al.
Journal of Neurodevelopmental Disorders
|
March 4, 2023
Comparison of evoked potentials across four related developmental encephalopathies
Joni N Saby, Sarika U Peters, Timothy A Benke, et al.
American Journal of Medical Genetics. Part A
|
November 10, 2020
Phenotypic features in MECP2 duplication syndrome: Effects of age
Sarika U Peters, Cary Fu, Eric D Marsh, et al.
Page
of 11