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Atypical ZFHX1B mutation associated with a mild Mowat–Wilson syndrome phenotype
Christiane Zweier, Denise Horn, Cornelia Kraus, Anita RauchVolume:
140A
Year:
2006
Language:
english
Pages:
4
DOI:
10.1002/ajmg.a.31196
File:
PDF, 161 KB
english, 2006