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cma-hr+snp v11.2 platform  (Baylor Genetics)

 
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    Baylor Genetics cma-hr+snp v11.2 platform
    Cma Hr+Snp V11.2 Platform, supplied by Baylor Genetics, 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/chromosomal+microarray+analysis/v11+2+chromosomal+microarray+analysis/pmc10081920-71-17-10
    Average 90 stars, based on 1 article reviews
    cma-hr+snp v11.2 platform - by Bioz Stars, 2026-11
    90/100 stars

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    Related Articles

    other:

    Article Title: Biallelic mutation of FBXL7 suggests a novel form of Hennekam syndrome.
    Article Snippet: Clinical microarray analysis (copy-number and SNP analysis) was performed by Baylor Genetics (https://www.bcm.edu/research/medical-genetics-labs/) using the CMA-HR + SNP V11.2 platform.

    Article Title: Biallelic mutation of FBXL7 suggests a novel form of Hennekam syndrome
    Article Snippet: Clinical microarray analysis (copy-number and SNP analysis) was performed by Baylor Genetics ( https://www.bcm.edu/research/medical-genetics-labs/ ) using the CMA-HR+SNP V11.2 platform.

    Article Title: Amish nemaline myopathy and dilated cardiomyopathy caused by a homozygous contiguous gene deletion of TNNT1 and TNNI3 in a Mennonite child
    Article Snippet: The patient was studied by V11.2 chromosomal microarray analysis designed by Baylor Genetics Laboratories and manufactured by Agilent Technology (Santa Clara, CA, USA).



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