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

Publisher： Karger

E-ISSN： 1424-859x|124|1|94-101

ISSN： 1424-8581

Source： Cytogenetic and Genome Research, Vol.124, Iss.1, 2009-04, pp. : 94-101

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