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Year | Number of Results |
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2014 | 3 |
2015 | 1 |
2025 | 0 |
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The prevalence of clinical features associated with primary ciliary dyskinesia in a heterotaxy population: results of a web-based survey.
Cardiol Young. 2015 Apr;25(4):752-9. doi: 10.1017/S1047951114000912. Epub 2014 Jun 6.
Cardiol Young. 2015.
PMID: 24905662
Free PMC article.
Laterality defects other than situs inversus totalis in primary ciliary dyskinesia: insights into situs ambiguus and heterotaxy.
Shapiro AJ, Davis SD, Ferkol T, Dell SD, Rosenfeld M, Olivier KN, Sagel SD, Milla C, Zariwala MA, Wolf W, Carson JL, Hazucha MJ, Burns K, Robinson B, Knowles MR, Leigh MW; Genetic Disorders of Mucociliary Clearance Consortium.
Shapiro AJ, et al.
Chest. 2014 Nov;146(5):1176-1186. doi: 10.1378/chest.13-1704.
Chest. 2014.
PMID: 24577564
Free PMC article.
Clinical Trial.
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Cri du chat syndrome and primary ciliary dyskinesia: a common genetic cause on chromosome 5p.
Shapiro AJ, Weck KE, Chao KC, Rosenfeld M, Nygren AO, Knowles MR, Leigh MW, Zariwala MA.
Shapiro AJ, et al.
J Pediatr. 2014 Oct;165(4):858-61. doi: 10.1016/j.jpeds.2014.06.048. Epub 2014 Jul 25.
J Pediatr. 2014.
PMID: 25066065
Free PMC article.
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