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A novel 5q11.2 deletion detected by microarray comparative genomic hybridisation in a child referred as a case of suspected 22q11 deletion syndrome

✍ Scribed by Katrina Prescott; Kathryn Woodfine; Paula Stubbs; Maurice Super; Bronwyn Kerr; Rodger Palmer; Nigel P. Carter; Peter Scambler

Publisher: Springer
Year: 2004
Tongue: English
Weight: 374 KB
Volume: 116
Category: Article
ISSN: 0340-6717
DOI: 10.1007/s00439-004-1195-6

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