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HGG Advances
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August 29, 2022
Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by <i>de novo</i> KCNC2 variants
Souhrid Mukherjee, Thomas A Cassini, Ningning Hu, et al.
Molecular Genetics & Genomic Medicine
|
December 17, 2025
Phenotypic Variability and Paternal Inheritance of a CHD8 Variant Causing Intellectual Developmental Disorder With Autism and Macrocephaly Confirmed by Epigenetic and Structural Analyses
Yutaka Furuta, Kimberly M Ezell, Rizwan Hamid, et al.
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Search research articles
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Showing results (11-20 of 12) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 12 results.
HGG Advances
|
August 29, 2022
Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by <i>de novo</i> KCNC2 variants
Souhrid Mukherjee, Thomas A Cassini, Ningning Hu, et al.
Molecular Genetics & Genomic Medicine
|
December 17, 2025
Phenotypic Variability and Paternal Inheritance of a CHD8 Variant Causing Intellectual Developmental Disorder With Autism and Macrocephaly Confirmed by Epigenetic and Structural Analyses
Yutaka Furuta, Kimberly M Ezell, Rizwan Hamid, et al.
Page
of 2