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Quest Diagnostics chromosomal microarray
Chromosomal Microarray, supplied by Quest Diagnostics, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/chromosomal+microarray/chromosomal+microarray/pm41795819-86-33-36
Average 86 stars, based on 1 article reviews
chromosomal microarray - by Bioz Stars, 2026-10
86/100 stars

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Related Articles

Microarray:

Article Title: Perinatal findings in a patient with a novel large chromosome 19p deletion
Article Snippet: .. High‐resolution chromosomal microarray showed a 3.7 Mb interstitial deletion of the short arm of chromosome 19, bands p13.2 p13.12 (11 836 342‐15 505 009)x1 (Quest Diagnostics Nichols Institute, Chantilly, VA). ..

Article Title: Genetic testing for the epilepsies: A systematic review.
Article Snippet: © 2021 International League Against Epilepsy Beth R. Sheidley and Jennifer Malinowski contributed equally to the study design, analysis, and manuscript development.. 1Epilepsy Genetics Program, Division of Epilepsy and Neurophysiology, Department of Neurology, Boston Children’s Hospital, Boston, Massachusetts, USA 2Write Inscite, South Salem, New York, USA 3Department of Genetics and Development, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York, USA 4Institute for Genomic Medicine, Columbia University Irving Medical Center, New York, New York, USA 5Department of Neurology, Charleston Area Medical Center, Charleston, West Virginia, USA 6Department of Genetic Medicine, Johns Hopkins University, Baltimore, Maryland, USA 7Department of Pathology, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York, USA 8Department of Neurology, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York, USA 9Genomics Services, Quest Diagnostics, Marlborough, Massachusetts, USA 10Department of Neurology, Harvard Medical School, Boston, Massachusetts, USA

Article Title: Double trouble: When focal and diffuse hyperinsulinism occur simultaneously.
Article Snippet: .. This patient had additional genetic testing due to her complex heart defect, including FISH for DiGeorge syndrome from Quest Diagnostics (negative), Noonan and Comprehensive RASopathies Panel/Sequencing and Deletion/Duplication Analysis from GeneDx (negative), and chromosomal microarray from Quest Diagnostics (227 kb deletion at 17p13.3, considered a variant of uncertain clinical significance). ..

Article Title: Rapid whole-genome sequencing identifies a novel GABRA1 variant associated with West syndrome
Article Snippet: .. A chromosomal microarray (Quest Diagnostics) revealed a likely benign 61-kb interstitial deletion at Chr 2p13.3, which encompasses the genes encoding F-box protein 48 ( FBX048 ) , aprataxin ( APTX ), and PNKP-like factor ( APLF ). .. Four days after consent for trio WGS, DNA was extracted and sequenced using an Illumina HiSeq X with paired 151-nt reads.

Sequencing:

Article Title: Genetic testing for the epilepsies: A systematic review.
Article Snippet: © 2021 International League Against Epilepsy Beth R. Sheidley and Jennifer Malinowski contributed equally to the study design, analysis, and manuscript development.. 1Epilepsy Genetics Program, Division of Epilepsy and Neurophysiology, Department of Neurology, Boston Children’s Hospital, Boston, Massachusetts, USA 2Write Inscite, South Salem, New York, USA 3Department of Genetics and Development, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York, USA 4Institute for Genomic Medicine, Columbia University Irving Medical Center, New York, New York, USA 5Department of Neurology, Charleston Area Medical Center, Charleston, West Virginia, USA 6Department of Genetic Medicine, Johns Hopkins University, Baltimore, Maryland, USA 7Department of Pathology, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York, USA 8Department of Neurology, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York, USA 9Genomics Services, Quest Diagnostics, Marlborough, Massachusetts, USA 10Department of Neurology, Harvard Medical School, Boston, Massachusetts, USA

Fluorescence In Situ Hybridization:

Article Title: Double trouble: When focal and diffuse hyperinsulinism occur simultaneously.
Article Snippet: .. This patient had additional genetic testing due to her complex heart defect, including FISH for DiGeorge syndrome from Quest Diagnostics (negative), Noonan and Comprehensive RASopathies Panel/Sequencing and Deletion/Duplication Analysis from GeneDx (negative), and chromosomal microarray from Quest Diagnostics (227 kb deletion at 17p13.3, considered a variant of uncertain clinical significance). ..

Variant Assay:

Article Title: Double trouble: When focal and diffuse hyperinsulinism occur simultaneously.
Article Snippet: .. This patient had additional genetic testing due to her complex heart defect, including FISH for DiGeorge syndrome from Quest Diagnostics (negative), Noonan and Comprehensive RASopathies Panel/Sequencing and Deletion/Duplication Analysis from GeneDx (negative), and chromosomal microarray from Quest Diagnostics (227 kb deletion at 17p13.3, considered a variant of uncertain clinical significance). ..



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