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Detection of a deletion of exons 8–16 of the UBE3A gene in familial Angelman syndrome using a semi-quantitative dosage PCR based assay

✍ Scribed by L. Boyes; A.J. Wallace; M. Krajewska-Walasek; K.H. Chrzanowska; J. Clayton-Smith; S. Ramsden


Book ID
116432993
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
829 KB
Volume
49
Category
Article
ISSN
1769-7212

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