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Paper Details

A New Family with a Novel <i>OTUD6B</i> Mutation: Practicing Whole Exome Sequencing for Antenatal Diagnosis of Tetralogy of Fallot.
Mol Syndromol
2
2022
Author NameAffiliation
H??lya KayseriliDiagnostic Center for Genetic Diseases, Koc University Hospital
H??lya KayseriliKoc University School of Medicine
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Datasets

Release 1.2