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Gene duplications in 21-hydroxylase deficiency: the importance of accurate molecular diagnosis in carrier detection and prenatal diagnosis
B. Ezquieta, M. Beneyto, R. Muñoz-Pacheco, R. Barrio, M. Oyarzabal, J. L. Lechuga, C. Luzuriaga, F. Hermoso, S. Quinteiro, S. MartinezVolume:
26
Year:
2006
Language:
english
Pages:
7
DOI:
10.1002/pd.1584
File:
PDF, 408 KB
english, 2006