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Quest Diagnostics oligonucleotide-snp chromosomal microarray
Oligonucleotide Snp Chromosomal Microarray, supplied by Quest Diagnostics, 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/oligonucleotide+chromosomal+microarray/clarisure++oligo+snp+chromosomal+microarray/pmc03468330-95-1-6
Average 90 stars, based on 1 article reviews
oligonucleotide-snp chromosomal microarray - by Bioz Stars, 2026-11
90/100 stars

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Article Title: Method and compositions for detecting an adenoma-adenocarcinoma transition in cancer
Article Snippet: One exemplary oligo-SNP array is the Genomic Alterations, Postnatal, ClariSure® Oligo-SNP Array (Quest Diagnostics, Madison, N.J.).

Article Title: Heterozygous Deletions in MKRN3 Cause Central Precocious Puberty Without Prader-Willi Syndrome
Article Snippet: Sixteen probands were tested for CNVs and regions of homozygosity by Oligo-SNP Chromosomal Microarray Analysis (CMA; ClariSure, Quest Diagnostics; 2.67 million probes).

Article Title: P622: NIPS dilemma in the context of consanguinity: Considerations for counseling
Article Snippet: ClariSure® Oligo-SNP chromosomal microarray with Quest Diagnostics™ on amniotic fluid revealed 46, XX with no copy number variants, but multiple ROHs (combined length ~24.5 Mb) encompassing chromosomes 5, 6, and 14.

Article Title: Genetic evaluation including exome sequencing of two patients with Gomez-Lopez-Hernandez syndrome: Case reports and review of the literature.
Article Snippet: Correspondence Faith Lindsay, Department of Pediatrics, University of Tennessee College of Medicine, Chattanooga, TN 37403.. Email: lindsayf@etsu.edu Abstract Rhombencephalosynapsis (RES) is a rare congenital anomaly of the hindbrain characterized by fusion of the cerebellar hemispheres, cerebellar peduncles, and dentate nuclei with vermian absence or hypogenesis.. This anomaly can be isolated or part of a larger spectrum of cerebral abnormalities.

Article Title: Unusual Trisomy X Phenotype Associated with a Concurrent Heterozygous 16p11.2 Deletion: Importance of an Integral Approach for Proper Diagnosis
Article Snippet: CMA (ClariSure ® Oligo-SNP, 2.67 million probes, Test code: 16478; Quest Diagnostics, Nichols Institute, Chantilly, VA, USA) confirmed trisomy X but also identified a heterozygous 304-kb deletion at 16p11.2 (arr[GRCh37] (X)x3,16p11.2(28,747,521_29,051,191)x1) ( a).

Article Title: Method and compositions for detecting an adenoma-adenocarcinoma transition in cancer
Article Snippet: One exemplary oligo-SNP array is the Genomic Alterations, Postnatal, ClariSure® Oligo-SNP Array (Quest Diagnostics, Madison, New Jersey).

Article Title: Unusual Trisomy X Phenotype Associated with a Concurrent Heterozygous 16p11.2 Deletion: Importance of an Integral Approach for Proper Diagnosis.
Article Snippet: CMA (ClariSure® Oligo-SNP, 2.67 million probes, Test code: 16478; Quest Diagnostics, Nichols In- stitute, Chantilly, VA, USA) confirmed trisomy X but also identified a heterozygous 304-kb deletion at 16p11.2 (arr[GRCh37] (X)x3,16p11.2(28,747,521_29,051,191)x1) (Figure 3a).



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