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Public Library of Science, PLoS ONE, 5(3), p. e2138, 2008

DOI: 10.1371/journal.pone.0002138

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High Frequency of Copy Number Variations and Sequence Variants at CYP21A2 Locus: Implication for the Genetic Diagnosis of 21-Hydroxylase Deficiency

Journal article published in 2008 by Silvia Parajes, Celsa Quinteiro, Fernando Domínguez ORCID, Lourdes Loidi
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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