Search research articles
Contact Us
Filters
Showing results (261-270 of 290) with videos related to
Page
of 29
Sort By:
American Journal of Human Genetics
|
October 5, 2019
De Novo Pathogenic Variants in N-cadherin Cause a Syndromic Neurodevelopmental Disorder with Corpus Collosum, Axon, Cardiac, Ocular, and Genital Defects
Andrea Accogli, Sara Calabretta, Judith St-Onge, et al.
Annals of Clinical and Translational Neurology
|
July 24, 2022
ANKLE2-related microcephaly: A variable microcephaly syndrome resembling Zika infection
Ajay X Thomas, Nichole Link, Laurie A Robak, et al.
American Journal of Human Genetics
|
June 15, 2007
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders
Francesco Brancati, Giuseppe Barrano, Jennifer L Silhavy, et al.
Developmental Cell
|
October 13, 2022
Loss of non-motor kinesin KIF26A causes congenital brain malformations via dysregulated neuronal migration and axonal growth as well as apoptosis
Xuyu Qian, Ellen M DeGennaro, Maya Talukdar, et al.
Journal of Medical Genetics
|
October 12, 2012
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders
Flore Zufferey, Elliott H Sherr, Noam D Beckmann, et al.
Nature Communications
|
November 3, 2022
Systematic analysis and prediction of genes associated with monogenic disorders on human chromosome X
Elsa Leitão, Christopher Schröder, Ilaria Parenti, et al.
Nature
|
May 21, 2025
Glioblastoma-instructed astrocytes suppress tumour-specific T cell immunity
Camilo Faust Akl, Brian M Andersen, Zhaorong Li, et al.
Science Advances
|
July 10, 2024
Monoallelic de novo <i>AJAP1</i> loss-of-function variants disrupt trans-synaptic control of neurotransmitter release
Simon Früh, Sami Boudkkazi, Peter Koppensteiner, et al.
American Journal of Human Genetics
|
June 29, 2021
Unique variants in CLCN3, encoding an endosomal anion/proton exchanger, underlie a spectrum of neurodevelopmental disorders
Anna R Duncan, Maya M Polovitskaya, Héctor Gaitán-Peñas, et al.
American Journal of Human Genetics
|
April 24, 2021
Missense variants in DPYSL5 cause a neurodevelopmental disorder with corpus callosum agenesis and cerebellar abnormalities
Médéric Jeanne, Hélène Demory, Aubin Moutal, et al.
Page
of 29
Search research articles
Search
Showing results (261-270 of 290) with videos related to
Sort By:
Page
of 29
American Journal of Human Genetics
|
October 5, 2019
De Novo Pathogenic Variants in N-cadherin Cause a Syndromic Neurodevelopmental Disorder with Corpus Collosum, Axon, Cardiac, Ocular, and Genital Defects
Andrea Accogli, Sara Calabretta, Judith St-Onge, et al.
Annals of Clinical and Translational Neurology
|
July 24, 2022
ANKLE2-related microcephaly: A variable microcephaly syndrome resembling Zika infection
Ajay X Thomas, Nichole Link, Laurie A Robak, et al.
American Journal of Human Genetics
|
June 15, 2007
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders
Francesco Brancati, Giuseppe Barrano, Jennifer L Silhavy, et al.
Developmental Cell
|
October 13, 2022
Loss of non-motor kinesin KIF26A causes congenital brain malformations via dysregulated neuronal migration and axonal growth as well as apoptosis
Xuyu Qian, Ellen M DeGennaro, Maya Talukdar, et al.
Journal of Medical Genetics
|
October 12, 2012
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders
Flore Zufferey, Elliott H Sherr, Noam D Beckmann, et al.
Nature Communications
|
November 3, 2022
Systematic analysis and prediction of genes associated with monogenic disorders on human chromosome X
Elsa Leitão, Christopher Schröder, Ilaria Parenti, et al.
Nature
|
May 21, 2025
Glioblastoma-instructed astrocytes suppress tumour-specific T cell immunity
Camilo Faust Akl, Brian M Andersen, Zhaorong Li, et al.
Science Advances
|
July 10, 2024
Monoallelic de novo <i>AJAP1</i> loss-of-function variants disrupt trans-synaptic control of neurotransmitter release
Simon Früh, Sami Boudkkazi, Peter Koppensteiner, et al.
American Journal of Human Genetics
|
June 29, 2021
Unique variants in CLCN3, encoding an endosomal anion/proton exchanger, underlie a spectrum of neurodevelopmental disorders
Anna R Duncan, Maya M Polovitskaya, Héctor Gaitán-Peñas, et al.
American Journal of Human Genetics
|
April 24, 2021
Missense variants in DPYSL5 cause a neurodevelopmental disorder with corpus callosum agenesis and cerebellar abnormalities
Médéric Jeanne, Hélène Demory, Aubin Moutal, et al.
Page
of 29