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whole-genome array-based comparative genomic hybridization (cgh)  (GeneDx Inc)

 
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    GeneDx Inc whole-genome array-based comparative genomic hybridization (cgh)
    Whole Genome Array Based Comparative Genomic Hybridization (Cgh), supplied by GeneDx Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/array-based+comparative+genomic+hybridization+(array-cgh/clinical+microarray+services/pm22091964-47-7-17
    Average 90 stars, based on 1 article reviews
    whole-genome array-based comparative genomic hybridization (cgh) - by Bioz Stars, 2026-09
    90/100 stars

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    Article Title: Diagnostic yield of advanced genetic testing in patients with hereditary neuropathies: A retrospective single-site study.
    Article Snippet: Correspondence Kevin J. Felice, Department of Neuromuscular Medicine, Hospital for Special Care, New Britain, CT 06053.. Email: felicek@hfsc.org Abstract Introduction/Aims: Advanced genetic testing including next-generation sequencing (AGT/NGS) has facilitated DNA testing in the clinical setting and greatly expanded new gene discovery for the Charcot-Marie-Tooth neuropathies and other hereditary neuropathies (CMT/HN).. Herein, we report AGT/NGS results, clinical findings, and diagnostic yield in a cohort of CMT/HN patients evaluated at our neuropathy care center.

    Article Title: A Patient Case of Malan Syndrome Involving 19p13.2 Deletion of NFIX with Longitudinal Follow-Up and Future Prospectives
    Article Snippet: Whole-genome array comparative genomic hybridization (CGH) and single-nucleotide polymorphism (SNP) analysis (GeneDx, Gaithersburg, MD) revealed the following: arr [GRCh37] 19p13.2 (13,180,583–13,255,428) × 1 de novo deletion of 75 kb ( ).

    Article Title: Functional Characterization of Biallelic RTTN Variants Identified in an Infant with Microcephaly, Simplified Gyral Pattern, Pontocerebellar Hypoplasia, and Seizures
    Article Snippet: Exon level oligo array comparative genomic hybridization (CGH) (ExonArrayDx) for the coding exons of the candidate gene was performed in a clinical laboratory (GeneDx, Gaithersburg, MD) on DNA obtained from the proband.

    Article Title: Novel Intragenic PAX6 Deletion in a Pedigree with Aniridia, Morbid Obesity, and Diabetes
    Article Snippet: OMIM #600958) gene, known to be associated with hypertrophic cardiomyopathy. ( 21 – 22 ) The specific breakpoints of this deletion were subsequently shown to encompass a 1.7 Mbp segment of chromosome 11 (46,842,700–48,588,943 bp) using a comparative genome hybridization (CGH) assay (GeneDx, Gaithersburg, MD).



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