Gene duplications in 21-hydroxylase deficiency: the importance of accurate molecular diagnosis in carrier detection and prenatal diagnosis
Ezquieta, B., Beneyto, M., Muñoz-Pacheco, R., Barrio, R., Oyarzabal, M., Lechuga, J. L., Luzuriaga, C., Hermoso, F., Quinteiro, S., Martinez, S.
Published in Prenatal diagnosis (01.12.2006)
Published in Prenatal diagnosis (01.12.2006)
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