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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
Author(s) -
Caignec Cédric Le,
Winer Norbert,
Philippe HenriJean,
Rival JeanMarie
Publication year - 2006
Publication title -
prenatal diagnosis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.956
H-Index - 97
eISSN - 1097-0223
pISSN - 0197-3851
DOI - 10.1002/pd.1499
Subject(s) - medical genetics , medicine , genetics , biology , gene
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