Detection of a novel familial deletion of four genes between BP1 and BP2 of the Prader-Willi/Angelman syndrome critical region by oligo-array CGH in a child with neurological disorder and speech impairment

Publisher： Karger

E-ISSN： 1424-859x|116|1-2|135-140

ISSN： 1424-8581

Source： Cytogenetic and Genome Research, Vol.116, Iss.1-2, 2007-02, pp. : 135-140

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