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Facial phenotype allows diagnosis of Mowat–Wilson syndrome in the absence of hirschsprung disease
Author(s) -
Horn Denise,
Weschke Bernhard,
Zweier Christiane,
Rauch Anita
Publication year - 2003
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.20298
Subject(s) - wilson's disease , phenotype , hirschsprung's disease , medicine , disease , gastroenterology , biology , genetics , gene
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