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 A. Talseth‐Palmer(New South Wales Department of Health), Rodney J. Scott(New South Wales Department of Health), S. Yu(Women's and Children's Hospital), Nikola A. Bowden(Hunter Medical Research Institute), Drago Bratkovic(Women's and Children's Hospital), Elizabeth Thompson(St. Jude Children's Research Hospital), Kathryn Friend(Women's and Children's Hospital), J. Nicholl(Women's and Children's Hospital), Jan Liebelt(South Australia Pathology), E Haan(Women's and Children's Hospital), Cliff Meldrum(New South Wales Department of Health)
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