PDF) Brief Report: Evaluating the Diagnostic Yield of Commercial Gene Panels in Autism
PDF) Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism
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Autism Genetic Testing | GeneDx
Syndromic Macrocephaly/Overgrowth Syndromes Panel Sequence Analysis and Exon-Level Deletion/Duplication Testing of 29 Genes
Peroxisomal Disorders Panel
Prenatal Limb Abnormalities Panel Sequence Analysis and Deletion/Duplication Testing of 5 Genes
AUTISM/ID PANEL
Clinical Exome Sequencing at GeneDx
Cost-effectiveness of genome-wide sequencing for unexplained developmental disabilities and multiple congenital anomalies | Genetics in Medicine
Genetic testing of TSC1 and TSC2 Genes in Tuberous Sclerosis Complex (TSC)
Lissencephaly Panel Sequence Analysis and Exon-Level Deletion/Duplication Testing of 26 Genes
Microcephaly Xpanded Panel
Novel founder intronic variant in SLC39A14 in two families causing Manganism and potential treatment strategies
GeneDx | Gaithersburg MD
GeneDx | LinkedIn
Frontiers | Next Generation Sequencing Methods for Diagnosis of Epilepsy Syndromes
Genetic testing including targeted gene panel in a diverse clinical population of children with autism spectrum disorder: Findings and implications – topic of research paper in Biological sciences. Download scholarly article PDF
GeneDx (@GeneDx) / Twitter
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GeneDx | Clinical Genomics | Genetic Testing | Rapid Results | GeneDx
Rubinstein-Taybi Syndrome (RSTS) Panel
GeneDx | Gaithersburg MD
