Literature DB >> 22232363

Genotyping in primary ciliary dyskinesia: ready for prime time, or a fringe benefit?

Claire Hogg, Andrew Bush.   

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Year:  2012        PMID： 22232363     DOI： 10.1136/thoraxjnl-2011-201320

Source DB:  PubMed          Journal:  Thorax        ISSN： 0040-6376            Impact factor:   9.139


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  4 in total

1.  Clinical and genetic analysis of a family with Kartagener syndrome caused by novel DNAH5 mutations.

Authors:  Xuan Xu; Ping Gong; Jie Wen
Journal:  J Assist Reprod Genet       Date:  2016-12-17       Impact factor: 3.412

2.  Primary ciliary dyskinesia: critical evaluation of clinical symptoms and diagnosis in patients with normal and abnormal ultrastructure.

Authors:  Mieke Boon; Anne Smits; Harry Cuppens; Martine Jaspers; Marijke Proesmans; Lieven J Dupont; Francois L Vermeulen; Sabine Van Daele; Anne Malfroot; Veronique Godding; Mark Jorissen; Kris De Boeck
Journal:  Orphanet J Rare Dis       Date:  2014-01-22       Impact factor: 4.123

3.  Reply to Shoemark et al. and to Shapiro et al.

Authors:  Israel Amirav; Moran Lavie
Journal:  Am J Respir Crit Care Med       Date:  2020-01-01       Impact factor: 21.405

4.  Accuracy of diagnostic testing in primary ciliary dyskinesia.

Authors:  Claire L Jackson; Laura Behan; Samuel A Collins; Patricia M Goggin; Elizabeth C Adam; Janice L Coles; Hazel J Evans; Amanda Harris; Peter Lackie; Samantha Packham; Anton Page; James Thompson; Woolf T Walker; Claudia Kuehni; Jane S Lucas
Journal:  Eur Respir J       Date:  2015-12-02       Impact factor: 16.671
  4 in total

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