Two independent rare events—a mutation in the RUNX2 gene and a de novo balanced translocation—in a fetus with cleidocranial dysplasia: pitfall in prenatal diagnosis
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Media type:
E-Article
Title:
Two independent rare events—a mutation in the RUNX2 gene and a de novo balanced translocation—in a fetus with cleidocranial dysplasia: pitfall in prenatal diagnosis