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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

✍ Scribed by Feng Li; Denise A.S. Batista; Irene Maumenee; Tao Wang


Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
97 KB
Volume
152A
Category
Article
ISSN
1552-4825

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