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Human Genetics
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June 30, 2017
Erratum to: Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features
Jing Zhang, Tomasz Gambin, Bo Yuan, et al.
Frontiers in Immunology
|
May 22, 2023
Chromosomal microarray analysis supplements exome sequencing to diagnose children with suspected inborn errors of immunity
Breanna J Beers, Morgan N Similuk, Rajarshi Ghosh, et al.
Genome Medicine
|
May 21, 2025
Untargeted proteomics enables ultra-rapid variant prioritisation in mitochondrial and other rare diseases
Daniella H Hock, Nikeisha J Caruana, Liana N Semcesen, et al.
Human Genetics
|
March 3, 2017
Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features
Jing Zhang, Tomasz Gambin, Bo Yuan, et al.
American Journal of Human Genetics
|
November 11, 2022
TCEAL1 loss-of-function results in an X-linked dominant neurodevelopmental syndrome and drives the neurological disease trait in Xq22.2 deletions
Hadia Hijazi, Linda M Reis, Davut Pehlivan, et al.
Genome Medicine
|
March 23, 2017
Lessons learned from additional research analyses of unsolved clinical exome cases
Mohammad K Eldomery, Zeynep Coban-Akdemir, Tamar Harel, et al.
American Journal of Human Genetics
|
March 28, 2017
Biallelic Variants in OTUD6B Cause an Intellectual Disability Syndrome Associated with Seizures and Dysmorphic Features
Teresa Santiago-Sim, Lindsay C Burrage, Frédéric Ebstein, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 7, 2021
Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalities
Fuad Chowdhury, Lei Wang, Mohammed Al-Raqad, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 31, 2018
Clinical exome sequencing reveals locus heterogeneity and phenotypic variability of cohesinopathies
Bo Yuan, Juanita Neira, Davut Pehlivan, et al.
Annals of Neurology
|
October 9, 2018
KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy-lysosome defect
Kyle A Metz, Xinchen Teng, Isabelle Coppens, et al.
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of 14
Search research articles
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Showing results (111-120 of 138) with videos related to
Sort By:
Page
of 14
Human Genetics
|
June 30, 2017
Erratum to: Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features
Jing Zhang, Tomasz Gambin, Bo Yuan, et al.
Frontiers in Immunology
|
May 22, 2023
Chromosomal microarray analysis supplements exome sequencing to diagnose children with suspected inborn errors of immunity
Breanna J Beers, Morgan N Similuk, Rajarshi Ghosh, et al.
Genome Medicine
|
May 21, 2025
Untargeted proteomics enables ultra-rapid variant prioritisation in mitochondrial and other rare diseases
Daniella H Hock, Nikeisha J Caruana, Liana N Semcesen, et al.
Human Genetics
|
March 3, 2017
Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features
Jing Zhang, Tomasz Gambin, Bo Yuan, et al.
American Journal of Human Genetics
|
November 11, 2022
TCEAL1 loss-of-function results in an X-linked dominant neurodevelopmental syndrome and drives the neurological disease trait in Xq22.2 deletions
Hadia Hijazi, Linda M Reis, Davut Pehlivan, et al.
Genome Medicine
|
March 23, 2017
Lessons learned from additional research analyses of unsolved clinical exome cases
Mohammad K Eldomery, Zeynep Coban-Akdemir, Tamar Harel, et al.
American Journal of Human Genetics
|
March 28, 2017
Biallelic Variants in OTUD6B Cause an Intellectual Disability Syndrome Associated with Seizures and Dysmorphic Features
Teresa Santiago-Sim, Lindsay C Burrage, Frédéric Ebstein, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 7, 2021
Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalities
Fuad Chowdhury, Lei Wang, Mohammed Al-Raqad, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 31, 2018
Clinical exome sequencing reveals locus heterogeneity and phenotypic variability of cohesinopathies
Bo Yuan, Juanita Neira, Davut Pehlivan, et al.
Annals of Neurology
|
October 9, 2018
KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy-lysosome defect
Kyle A Metz, Xinchen Teng, Isabelle Coppens, et al.
Page
of 14