DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Pebrel-Richard C, Rouzade C, Kemeny S. , et al.
Refinement of the critical region in a new 7p22.1 microduplication syndrome including craniofacial dysmorphism and speech delay.
Am J Med Genet A 2014;
164A (11) 2964-2967
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