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Carrier status for 3 most frequent CFTR mutations in Polish PCD/KS patients: lack of association with the primary ciliary dyskinesia phenotype - Original article
Carrier status for 3 most frequent CFTR mutations in Polish PCD/KS patients: lack of association with the primary ciliary dyskinesia phenotype - Original article
Carrier status for 3 most frequent CFTR mutations in Polish PCD/KS patients: lack of association with the primary ciliary dyskinesia phenotype - Original article
Skrzypczak, U. (author) / Rutkiewicz, E. (author) / Pogorzelski, A. (author) / Witt, M. (author) / Zietkiewicz, E. (author)
JOURNAL OF APPLIED GENETICS ; 48 ; 85-88
2007-01-01
4 pages
Article (Journal)
English
DDC:
576.5
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