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Brain : a Journal of Neurology
|
March 18, 2019
Heterogeneous clinical phenotypes and cerebral malformations reflected by rotatin cellular dynamics
Laura V Vandervore, Rachel Schot, Esmee Kasteleijn, et al.
American Journal of Human Genetics
|
September 26, 2017
Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and Speech Delay, Postnatal Microcephaly, and Dysmorphic Features
Paweł Stankiewicz, Tahir N Khan, Przemyslaw Szafranski, 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.
The Lancet. Neurology
|
December 3, 2013
The genetic basis of DOORS syndrome: an exome-sequencing study
Philippe M Campeau, Dalia Kasperaviciute, James T Lu, et al.
Human Mutation
|
November 12, 2014
Variants in CUL4B are associated with cerebral malformations
Anneke T Vulto-van Silfhout, Tadashi Nakagawa, Nadia Bahi-Buisson, et al.
Nature Genetics
|
April 10, 2025
Mutations in the small nuclear RNA gene RNU2-2 cause a severe neurodevelopmental disorder with prominent epilepsy
Daniel Greene, Koenraad De Wispelaere, Jon Lees, et al.
American Journal of Human Genetics
|
April 17, 2018
A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar Dysgenesis
Heather E Olson, Nolwenn Jean-Marçais, Edward Yang, et al.
American Journal of Human Genetics
|
October 6, 2018
A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar Dysgenesis
Heather E Olson, Nolwenn Jean-Marçais, Edward Yang, et al.
Nature Communications
|
November 17, 2020
Germline AGO2 mutations impair RNA interference and human neurological development
Davor Lessel, Daniela M Zeitler, Margot R F Reijnders, et al.
Nature Genetics
|
May 27, 2017
Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia
Esther Meyer, Keren J Carss, Julia Rankin, et al.
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Search research articles
Search
Showing results (41-50 of 54) with videos related to
Sort By:
Page
of 6
Brain : a Journal of Neurology
|
March 18, 2019
Heterogeneous clinical phenotypes and cerebral malformations reflected by rotatin cellular dynamics
Laura V Vandervore, Rachel Schot, Esmee Kasteleijn, et al.
American Journal of Human Genetics
|
September 26, 2017
Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and Speech Delay, Postnatal Microcephaly, and Dysmorphic Features
Paweł Stankiewicz, Tahir N Khan, Przemyslaw Szafranski, 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.
The Lancet. Neurology
|
December 3, 2013
The genetic basis of DOORS syndrome: an exome-sequencing study
Philippe M Campeau, Dalia Kasperaviciute, James T Lu, et al.
Human Mutation
|
November 12, 2014
Variants in CUL4B are associated with cerebral malformations
Anneke T Vulto-van Silfhout, Tadashi Nakagawa, Nadia Bahi-Buisson, et al.
Nature Genetics
|
April 10, 2025
Mutations in the small nuclear RNA gene RNU2-2 cause a severe neurodevelopmental disorder with prominent epilepsy
Daniel Greene, Koenraad De Wispelaere, Jon Lees, et al.
American Journal of Human Genetics
|
April 17, 2018
A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar Dysgenesis
Heather E Olson, Nolwenn Jean-Marçais, Edward Yang, et al.
American Journal of Human Genetics
|
October 6, 2018
A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar Dysgenesis
Heather E Olson, Nolwenn Jean-Marçais, Edward Yang, et al.
Nature Communications
|
November 17, 2020
Germline AGO2 mutations impair RNA interference and human neurological development
Davor Lessel, Daniela M Zeitler, Margot R F Reijnders, et al.
Nature Genetics
|
May 27, 2017
Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia
Esther Meyer, Keren J Carss, Julia Rankin, et al.
Page
of 6