Clinical and Genetic Spectrum of Children With Primary Ciliary Dyskinesia in China-Reference-Cited by-同舟云学术

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Clinical and Genetic Spectrum of Children With Primary Ciliary Dyskinesia in China

Published:2021-05 Issue:5 Volume:159 Page:1768-1781
ISSN:0012-3692
Container-title:Chest
language:en
Short-container-title:Chest

Author:

Guan Yuhong,Yang Haiming,Yao Xingfeng,Xu Hui,Liu Hui,Tang Xiaolei,Hao Chanjuan,Zhang Xiang,Zhao Shunying,Ge Wentong,Ni Xin

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Critical Care and Intensive Care Medicine,Pulmonary and Respiratory Medicine

Reference40 articles.

1. Congenital heart disease and other heterotaxic defects in a large cohort of patients with primary ciliary dyskinesia;Kennedy;Circulation,2007

2. Advances in the genetics of primary ciliary dyskinesia: clinical implications;Horani;Chest,2018

3. Primary ciliary dyskinesia in the genomics age;Lucas;Lancet Respir Med,2020

4. Clinical utility of NGS diagnosis and disease stratification in a multiethnic primary ciliary dyskinesia cohort;Fassad;J Med Genet,2020

5. Genotype and phenotype evaluation of patients with primary ciliary dyskinesia: first results from Turkey;Emiralioğlu;Pediatr Pulmonol,2020

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4. A novel homozygous LRRC6 mutation causes male infertility with asthenozoospermia and primary ciliary dyskinesia in humans;Andrology;2024-06-27

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