Identification and characterization of three large deletions and a deletion/polymorphism in the CFTR gene
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Cited by 20 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. Cystic Fibrosis assessment in infertile couples: genetic analysis trough the Next Generation Sequencing technique;Clinical and Experimental Obstetrics & Gynecology;2022-05-06
2. Homozygous Deletion of the CFTR Gene Caused by Interstitial Maternal Isodisomy in a Peruvian Child with Cystic Fibrosis;Journal of Pediatric Genetics;2019-02-13
3. CFTR-France, a national relational patient database for sharing genetic and phenotypic data associated with rareCFTRvariants;Human Mutation;2017-06-28
4. Next generation diagnostics of cystic fibrosis andCFTR-related disorders by targeted multiplex high-coverage resequencing ofCFTR;Journal of Medical Genetics;2013-05-17
5. CFTR Rearrangements in Spanish Cystic Fibrosis Patients: First New Duplication (35kb) Characterised in the Mediterranean Countries;Annals of Human Genetics;2010-08-15
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