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A female patient with X‐linked Ohdo syndrome of the Maat‐Kievit‐Brunner phenotype caused by a novel variant of MED12
Author(s) -
Murakami Hiroaki,
Enomoto Yumi,
Tsurusaki Yoshinori,
Sugio Yoshitsugu,
Kurosawa Kenji
Publication year - 2020
Publication title -
congenital anomalies
Language(s) - English
Resource type - Journals
eISSN - 1741-4520
pISSN - 0914-3505
DOI - 10.1111/cga.12350
Subject(s) - phenotype , content (measure theory) , clinical phenotype , genetics , biology , medicine , gene , mathematics , mathematical analysis