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International Journal of Molecular Sciences
|
August 27, 2021
Identification of a DNA Methylation Episignature in the 22q11.2 Deletion Syndrome
Kathleen Rooney, Michael A Levy, Sadegheh Haghshenas, et al.
Clinical Genetics
|
May 18, 2023
Sleep disturbances in Phelan-McDermid syndrome: Clinical and metabolic profiling of 56 individuals
Bridgette A Moffitt, Lindsay M Oberman, Laura Beamer, et al.
American Journal of Medical Genetics. Part A
|
December 5, 2012
Clinical utility of the X-chromosome array
Yuri A Zarate, Alka Dwivedi, Frank O Bartel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 16, 2024
A multicenter analysis of individuals with a 47,XXY/46,XX karyotype
Tiffany Guess, Ferrin C Wheeler, Ashwini Yenamandra, et al.
Elife
|
December 22, 2020
<i>KDM5A</i> mutations identified in autism spectrum disorder using forward genetics
Lauretta El Hayek, Islam Oguz Tuncay, Nadine Nijem, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 27, 2021
Correction: Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders
Bekim Sadikovic, Michael A Levy, Jennifer Kerkhof, et al.
HGG Advances
|
August 25, 2024
LARP1 haploinsufficiency is associated with an autosomal dominant neurodevelopmental disorder
James Chettle, Raymond J Louie, Olivia Larner, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 6, 2021
Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders
Bekim Sadikovic, Michael A Levy, Jennifer Kerkhof, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 22, 2024
Diagnostic utility and reporting recommendations for clinical DNA methylation episignature testing in genetically undiagnosed rare diseases
Jennifer Kerkhof, Cassandra Rastin, Michael A Levy, et al.
Space Science Reviews
|
December 29, 2025
The IMAP-Ultra Energetic Neutral Atom (ENA) Imager
Matina Gkioulidou, G B Clark, D G Mitchell, et al.
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of 14
Search research articles
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Showing results (121-130 of 135) with videos related to
Sort By:
Page
of 14
International Journal of Molecular Sciences
|
August 27, 2021
Identification of a DNA Methylation Episignature in the 22q11.2 Deletion Syndrome
Kathleen Rooney, Michael A Levy, Sadegheh Haghshenas, et al.
Clinical Genetics
|
May 18, 2023
Sleep disturbances in Phelan-McDermid syndrome: Clinical and metabolic profiling of 56 individuals
Bridgette A Moffitt, Lindsay M Oberman, Laura Beamer, et al.
American Journal of Medical Genetics. Part A
|
December 5, 2012
Clinical utility of the X-chromosome array
Yuri A Zarate, Alka Dwivedi, Frank O Bartel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 16, 2024
A multicenter analysis of individuals with a 47,XXY/46,XX karyotype
Tiffany Guess, Ferrin C Wheeler, Ashwini Yenamandra, et al.
Elife
|
December 22, 2020
<i>KDM5A</i> mutations identified in autism spectrum disorder using forward genetics
Lauretta El Hayek, Islam Oguz Tuncay, Nadine Nijem, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 27, 2021
Correction: Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders
Bekim Sadikovic, Michael A Levy, Jennifer Kerkhof, et al.
HGG Advances
|
August 25, 2024
LARP1 haploinsufficiency is associated with an autosomal dominant neurodevelopmental disorder
James Chettle, Raymond J Louie, Olivia Larner, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 6, 2021
Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders
Bekim Sadikovic, Michael A Levy, Jennifer Kerkhof, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 22, 2024
Diagnostic utility and reporting recommendations for clinical DNA methylation episignature testing in genetically undiagnosed rare diseases
Jennifer Kerkhof, Cassandra Rastin, Michael A Levy, et al.
Space Science Reviews
|
December 29, 2025
The IMAP-Ultra Energetic Neutral Atom (ENA) Imager
Matina Gkioulidou, G B Clark, D G Mitchell, et al.
Page
of 14