array-cgh analysis (Oxford Gene Technology)
90
Structured Review
Oxford Gene Technology
array-cgh analysis
Array Cgh Analysis, supplied by Oxford Gene Technology, 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+cgh/cgh+array/pmc07310047-79-0-5
Average 90 stars, based on 1 article reviews
Array Cgh Analysis, supplied by Oxford Gene Technology, 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+cgh/cgh+array/pmc07310047-79-0-5
Average 90 stars, based on 1 article reviews
array-cgh analysis - by Bioz Stars,
2026-10
90/100 stars
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other:Article Title: Prostaglandin E 2 -EP 3 receptor subtype gene deletion in mother and son impairs platelet aggregation. Article Snippet: Array-comparative genomic hybridisation (CGH) was performed by an external laboratory (Rigshospitalet, Copenhagen, Denmark) for Patient 1, while array-CGH for Patient 2 was performed in house with Article Title: Prostaglandin E 2 -EP 3 receptor subtype gene deletion in mother and son impairs platelet aggregation. Article Snippet: Array-comparative genomic hybridisation (CGH) was performed by an external laboratory (Rigshospitalet, Copenhagen, Denmark) for Patient 1, while array-CGH for Patient 2 was performed in house with Article Title: Structural Variants in COL1A1 and COL1A2 in Osteogenesis Imperfecta. Article Snippet: Dosage abnormalities were initially detected using MLPA (probekit P271- B2 for COL1A1 and P272- B2 for COL1A2, MRC- Holland, Netherlands) and Article Title: Inherited duplication of the pseudoautosomal region Xq28 in a subject with Gilles de la Tourette syndrome and intellectual disability: a case report Article Snippet: Array-CGH analysis, performed using the Article Title: De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature Article Snippet: Array-CGH Array-comparative genomic hybridization analysis (CGH) was performed using Oxford Gene Technology Hybridization:Article Title: Dominantly inherited distal nemaline/cap myopathy caused by a large deletion in the nebulin gene. Article Snippet: The NEB haplotypes for the family were constructed using single nucleotide polymorphisms (SNPs) in the exons 4, 10, 31, 65, 122, 151, 173 and 181 for all the 13 family members from whom DNA samples were available (three affected and 10 unaffected family members) (Fig. 1). .. The Article Title: Histopathological Comparison of Eyes from Patients with Autosomal Recessive Retinitis Pigmentosa caused by novel EYS Mutations Article Snippet: .. To further search for the second pathogenic variation, the DNA was analyzed using a comparative Microarray:Article Title: Dominantly inherited distal nemaline/cap myopathy caused by a large deletion in the nebulin gene. Article Snippet: The NEB haplotypes for the family were constructed using single nucleotide polymorphisms (SNPs) in the exons 4, 10, 31, 65, 122, 151, 173 and 181 for all the 13 family members from whom DNA samples were available (three affected and 10 unaffected family members) (Fig. 1). .. The |