(Q51909598)
Statements
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An unbalanced translocation between chromosomes 2p and 6p associated with Axenfeld-Rieger anomaly type 3, hearing loss, developmental delay, and distinct facial dysmorphism. (English)
1 reference
Feng Li
1 reference
Denise A S Batista
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Irene Maumenee
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Tao Wang
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1 May 2010
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152A
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5
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1318-1321
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Identifiers
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1 reference