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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
Cédric Le Caignec, Norbert Winer, Henri-Jean Philippe, Jean-Marie Rival1Volume:
26
Year:
2006
Language:
english
Pages:
2
DOI:
10.1002/pd.1499
File:
PDF, 73 KB
english, 2006