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High frequency of copy number variations (CNVs) in the chromosome 11p15 region in patients with Beckwith–Wiedemann syndrome

✍ Scribed by Baskin, Berivan; Choufani, Sanaa; Chen, Yi-an; Shuman, Cheryl; Parkinson, Nicole; Lemyre, Emmanuelle; Micheil Innes, A.; Stavropoulos, Dimitri J.; Ray, Peter N.; Weksberg, Rosanna


Book ID
121554686
Publisher
Springer
Year
2013
Tongue
English
Weight
470 KB
Volume
133
Category
Article
ISSN
0340-6717

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