Loci for primary ciliary dyskinesia map to chromosome 16p12.1-12.2 and 15q13.1-15.1 in Faroe Islands and Israeli Druze genetic isolates
Author:
Publisher
BMJ
Subject
Genetics (clinical),Genetics
Cited by 33 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Identification of a frame shift mutation in the CCDC151 gene in a Han-Chinese family with Kartagener syndrome;Bioscience Reports;2020-06
2. Teratozoospermia: spotlight on the main genetic actors in the human;Human Reproduction Update;2015-04-17
3. Variation in DNAH1 may contribute to primary ciliary dyskinesia;BMC Medical Genetics;2015-03-17
4. CCDC40 mutation as a cause of primary ciliary dyskinesia: a case report and review of literature;The Clinical Respiratory Journal;2015-03-03
5. Unexpected genetic heterogeneity for primary ciliary dyskinesia in the Irish Traveller population;European Journal of Human Genetics;2014-05-14
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