De novo deletions and duplications of 17q25.3 cause...

Orphanet Journal of Rare Diseases 2015 / 12 Vol. 10; Iss. 1

De novo deletions and duplications of 17q25.3 cause susceptibility to cardiovascular malformations

Probst, F. J., James, R. A., Burrage, L. C., Rosenfeld, J. A., Bohan, T. P., Melver, C. H. Ward, Magoulas, P., Austin, E., Franklin, A. I. A., Azamian, M., Xia, F., Patel, A., Bi, W., Bacino, C., Belm
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Volume:
10
Language:
english
Journal:
Orphanet Journal of Rare Diseases
DOI:
10.1186/s13023-015-0291-0
Date:
December, 2015
File:
PDF, 2.38 MB
english, 2015
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