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Array comparative genomic hybridization characterization of multiple interstitial deletions involving 7p22.1, 7q11.23, 7q21.3-q22.1, 19p13.3-p12, and 19q13.11-q13.43 in a fetus associated with split hand–foot malformation. Role of EPS15L1 in pathogenesis

oleh: Ya-Lien Hsueh, Yi-Ning Su, Hsin-Yu Lin, Chien-Nan Lee, Jin-Chung Shih