Two Novel Missense Mutations (R766M and R792G) in Exon 13 of the CFTR Gene in a Patient with Congenital Bilateral Absence of the Vas deferens

Publisher： Karger

E-ISSN： 1423-0062|50|5|318-319

ISSN： 0001-5652

Source： Human Heredity, Vol.50, Iss.5, 2000-06, pp. : 318-319

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