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Comprehensive and Rapid Genotyping of Mutations and Haplotypes in Congenital Bilateral Absence of the Vas Deferens and Other Cystic Fibrosis Transmembrane Conductance Regulator-Related Disorders

✍ Scribed by Bareil, Corinne; Guittard, Caroline; Altieri, Jean-Pierre; Templin, Carine; Claustres, Mireille; des Georges, Marie

No coin nor oath required. For personal study only.

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