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Q47210500-9E8A6367-1712-4DAC-A73C-C066DEFC309C
Q47210500-9E8A6367-1712-4DAC-A73C-C066DEFC309C
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http://www.wikidata.org/entity/statement/Q47210500-9E8A6367-1712-4DAC-A73C-C066DEFC309C
Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care.
P2860
Q47210500-9E8A6367-1712-4DAC-A73C-C066DEFC309C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47210500-9E8A6367-1712-4DAC-A73C-C066DEFC309C
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wasDerivedFrom
344f80f3df501c8392c44862ab2b9fbcd2c9c50b
P2860
Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23