A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology.

Bente Talseth-Palmer, Nikola Bowden, Cliff Meldrum, Jillian Nicholl, Elizabeth Thompson, K Friend, J Liebelt, Drago Bratkovic, Eric Haan, S Yu, Rodney Scott

    Research output: Contribution to journalArticlepeer-review

    6 Citations (Scopus)
    Original languageEnglish
    Pages (from-to)94-101
    Number of pages8
    JournalCYTOGENETIC AND GENOME RESEARCH
    Volume124
    Issue number1
    Publication statusPublished - 2009

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