High frequency of copy number variations and sequence variants at CYP21A2 locus: implication for the genetic diagnosis of 21-hydroxylase deficiency (Q33334349)
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English | High frequency of copy number variations and sequence variants at CYP21A2 locus: implication for the genetic diagnosis of 21-hydroxylase deficiency |
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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 (English)
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Silvia Parajes
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Celsa Quinteiro
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Fernando DomÃnguez
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Lourdes Loidi
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14 May 2008
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e2138
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