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Medrxiv : the Preprint Server for Health Sciences
|
July 3, 2023
Loss-of-function variants in <i>CUL3</i> cause a syndromic neurodevelopmental disorder
Patrick R Blackburn, Frédéric Ebstein, Tzung-Chien Hsieh, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 8, 2024
Unique Capabilities of Genome Sequencing for Rare Disease Diagnosis
Monica H Wojcik, Gabrielle Lemire, Maha S Zaki, et al.
Annals of Neurology
|
September 20, 2024
Loss-of-Function Variants in CUL3 Cause a Syndromic Neurodevelopmental Disorder
Patrick R Blackburn, Frédéric Ebstein, Tzung-Chien Hsieh, et al.
Developmental Cell
|
April 2, 2019
The Pediatric Cell Atlas: Defining the Growth Phase of Human Development at Single-Cell Resolution
Deanne M Taylor, Bruce J Aronow, Kai Tan, et al.
American Journal of Medical Genetics. Part A
|
October 24, 2020
Alternative genomic diagnoses for individuals with a clinical diagnosis of Dubowitz syndrome
David A Dyment, Anne O'Donnell-Luria, Pankaj B Agrawal, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 4, 2021
Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior
Holly K Harris, Tojo Nakayama, Jenny Lai, et al.
Brain : a Journal of Neurology
|
September 26, 2020
Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia
Darius Ebrahimi-Fakhari, Julian Teinert, Robert Behne, et al.
The New England Journal of Medicine
|
June 5, 2024
Genome Sequencing for Diagnosing Rare Diseases
Monica H Wojcik, Gabrielle Lemire, Eva Berger, et al.
American Journal of Human Genetics
|
November 4, 2017
De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability
Sébastien Küry, Geeske M van Woerden, Thomas Besnard, et al.
American Journal of Human Genetics
|
July 10, 2026
Clinical, in vitro, and in vivo evidence of WAPL as a cohesinopathy-associated gene and phenotypic driver of 10q22.3q23.2 genomic disorder
Philip M Boone, Serkan Erdin, Abucar Mohamed, et al.
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Search research articles
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Showing results (351-360 of 360) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 360 results.
Medrxiv : the Preprint Server for Health Sciences
|
July 3, 2023
Loss-of-function variants in <i>CUL3</i> cause a syndromic neurodevelopmental disorder
Patrick R Blackburn, Frédéric Ebstein, Tzung-Chien Hsieh, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 8, 2024
Unique Capabilities of Genome Sequencing for Rare Disease Diagnosis
Monica H Wojcik, Gabrielle Lemire, Maha S Zaki, et al.
Annals of Neurology
|
September 20, 2024
Loss-of-Function Variants in CUL3 Cause a Syndromic Neurodevelopmental Disorder
Patrick R Blackburn, Frédéric Ebstein, Tzung-Chien Hsieh, et al.
Developmental Cell
|
April 2, 2019
The Pediatric Cell Atlas: Defining the Growth Phase of Human Development at Single-Cell Resolution
Deanne M Taylor, Bruce J Aronow, Kai Tan, et al.
American Journal of Medical Genetics. Part A
|
October 24, 2020
Alternative genomic diagnoses for individuals with a clinical diagnosis of Dubowitz syndrome
David A Dyment, Anne O'Donnell-Luria, Pankaj B Agrawal, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 4, 2021
Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior
Holly K Harris, Tojo Nakayama, Jenny Lai, et al.
Brain : a Journal of Neurology
|
September 26, 2020
Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia
Darius Ebrahimi-Fakhari, Julian Teinert, Robert Behne, et al.
The New England Journal of Medicine
|
June 5, 2024
Genome Sequencing for Diagnosing Rare Diseases
Monica H Wojcik, Gabrielle Lemire, Eva Berger, et al.
American Journal of Human Genetics
|
November 4, 2017
De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability
Sébastien Küry, Geeske M van Woerden, Thomas Besnard, et al.
American Journal of Human Genetics
|
July 10, 2026
Clinical, in vitro, and in vivo evidence of WAPL as a cohesinopathy-associated gene and phenotypic driver of 10q22.3q23.2 genomic disorder
Philip M Boone, Serkan Erdin, Abucar Mohamed, et al.
Page
of 36