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emarray cyto6000 oligonucleotide-based chromosomal microarray analysis  (Michigan Medical Genetics Laboratories)

 
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    Structured Review

    Michigan Medical Genetics Laboratories emarray cyto6000 oligonucleotide-based chromosomal microarray analysis
    Emarray Cyto6000 Oligonucleotide Based Chromosomal Microarray Analysis, supplied by Michigan Medical Genetics Laboratories, 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+analysis/emarray+cyto6000/pmc03160635-76-4-9
    Average 90 stars, based on 1 article reviews
    emarray cyto6000 oligonucleotide-based chromosomal microarray analysis - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    other:

    Article Title: Deletion at chromosomal band Xp22.12-Xp22.13 involving PDHA1 in a patient with congenital lactic acidosis.
    Article Snippet: We present a patient with congenital lactic acidosis, agenesis of the corpus callosum, and profound developmental delay.. Assays of pyruvate dehydrogenase complex function were normal in lymphocytes, but decreased in fibroblasts.. Sequencing of the PDHA1 gene did not reveal deleterious mutations, and BAC based microarray analysis did not reveal any chromosomal abnormality.

    Microarray:

    Article Title: Duplication 16p11.2 in a child with infantile seizure disorder.
    Article Snippet: .. An EMArray Cyto6000 oligonucleotide-based chromosomal microarray analysis at the Michigan Medical Genetics Laboratories (MMGL) revealed a de novo 598 kb duplication of 16p11.2. ..

    Article Title: Duplication 16p11.2 in a Child with Infantile Seizure Disorder
    Article Snippet: .. An EMArray Cyto6000 oligonucleotide-based chromosomal microarray analysis at the Michigan Medical Genetics Laboratories (MMGL) revealed a de novo 598 Kb duplication of 16p11.2. ..



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