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For:	Skrzypczak U, Rutkiewicz E, Pogorzelski A, Witt M, Zietkiewicz E. Carrier status for 3 most frequent CFTR mutations in Polish PCD/KS patients: lack of association with the primary ciliary dyskinesia phenotype. J Appl Genet 2007;48:85-8. [PMID: 17272866 DOI: 10.1007/BF03194662] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.2] [Reference Citation Analysis]

For:

Skrzypczak U, Rutkiewicz E, Pogorzelski A, Witt M, Zietkiewicz E. Carrier status for 3 most frequent CFTR mutations in Polish PCD/KS patients: lack of association with the primary ciliary dyskinesia phenotype. J Appl Genet 2007;48:85-8. [PMID: 17272866 DOI: 10.1007/BF03194662] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.2] [Reference Citation Analysis]

Number	Citing Articles
1	Cho DY, Hwang PH, Illek B. Characteristics of chloride transport in nasal mucosa from patients with primary ciliary dyskinesia. Laryngoscope 2010;120:1460-4. [PMID: 20564725 DOI: 10.1002/lary.20928] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis]
2	Ziętkiewicz E, Bukowy-Bieryłło Z, Voelkel K, Klimek B, Dmeńska H, Pogorzelski A, Sulikowska-Rowińska A, Rutkiewicz E, Witt M. Mutations in radial spoke head genes and ultrastructural cilia defects in East-European cohort of primary ciliary dyskinesia patients. PLoS One 2012;7:e33667. [PMID: 22448264 DOI: 10.1371/journal.pone.0033667] [Cited by in Crossref: 45] [Cited by in F6Publishing: 39] [Article Influence: 4.5] [Reference Citation Analysis]