Original language | English |
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Pages (from-to) | 94-101 |
Number of pages | 8 |
Journal | CYTOGENETIC AND GENOME RESEARCH |
Volume | 124 |
Issue number | 1 |
Publication status | Published - 2009 |
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 journal › Article › peer-review
6
Citations
(Scopus)