bibliographicCitation |
Parajes S, Quinteiro C, DomÃnguez F, Loidi L. High Frequency of Copy Number Variations and Sequence Variants at CYP21A2 Locus: Implication for the Genetic Diagnosis of 21-Hydroxylase Deficiency. PLoS ONE. 2008 May 14;3(5):e2138. doi: 10.1371/journal.pone.0002138. |