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Frontiers in Neurology
|
June 6, 2019
Diagnostic Yield and Treatment Impact of Targeted Exome Sequencing in Early-Onset Epilepsy
Michelle Demos, Ilaria Guella, Conrado DeGuzman, et al.
BMC Genomics
|
November 18, 2009
Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization
Jm Friedman, Shelin Adam, Laura Arbour, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 28, 2026
Multimodal Genotype-Phenotype Analysis in SMARCB1-Associated Developmental Disorders
Ramy Saad, Clementina Cobolli Gigli, Pleuntje J van der Sluijs, et al.
HGG Advances
|
May 23, 2022
Genome-wide sequencing and the clinical diagnosis of genetic disease: The CAUSES study
Alison M Elliott, Shelin Adam, Christèle du Souich, et al.
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Search research articles
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Showing results (31-40 of 34) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 34 results.
Frontiers in Neurology
|
June 6, 2019
Diagnostic Yield and Treatment Impact of Targeted Exome Sequencing in Early-Onset Epilepsy
Michelle Demos, Ilaria Guella, Conrado DeGuzman, et al.
BMC Genomics
|
November 18, 2009
Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization
Jm Friedman, Shelin Adam, Laura Arbour, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 28, 2026
Multimodal Genotype-Phenotype Analysis in SMARCB1-Associated Developmental Disorders
Ramy Saad, Clementina Cobolli Gigli, Pleuntje J van der Sluijs, et al.
HGG Advances
|
May 23, 2022
Genome-wide sequencing and the clinical diagnosis of genetic disease: The CAUSES study
Alison M Elliott, Shelin Adam, Christèle du Souich, et al.
Page
of 4