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A de novo KMT2D mutation in a girl with Kabuki syndrome associated with endocrine symptoms: a case report
Moon, Jung-Eun, Lee, Su-Jeong, Ko, Cheol WooVolume:
19
Language:
english
Journal:
BMC Medical Genetics
DOI:
10.1186/s12881-018-0606-9
Date:
December, 2018
File:
PDF, 466 KB
english, 2018