Cystic fibrosis mutations and immotile cilia syndrome-Reference-Cited by-同舟云学术

Cystic fibrosis mutations and immotile cilia syndrome

Published:2008-04-23 Issue:6 Volume:47 Page:328-329
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Liechti-Gallati Sabina,Kraemer Richard

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1995.tb03975.x/fullpdf

Reference16 articles.

1. HLA haplotype segregation and ultrastructural study in familial immotile-cilia syndrome;Bianchi;Hum Genet,1992

2. Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients;Dean;Cell,1990

3. Screening for non-deltaF508 mutations in five exons of the cystic fibrosis transmembrane conductance regulator (CFTR) gene in Italy;Devoto;Am J Hum Genet,1991

4. Abnormal distribution of cystic fibrosis ΔF508 allele in adults with chronic bronchial hypersecretion;Dumur;Lancet,1990

5. Detecting multiple cystic fibrosis mutations by polymerase chain reaction-mediated site-directed mutagenesis;Friedman;Clin Chem,1991

Cited by 3 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. Carrier status for 3 most frequentCFTR mutations in Polish PCD/KS patients: lack of association with the primary ciliary dyskinesia phenotype;Journal of Applied Genetics;2007-03

2. CLINICAL IMPLICATIONS OF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR MUTATIONS;Clinics in Chest Medicine;1998-09

3. Paternal Isodisomy of Chromosome 7 Associated with Complete Situs Inversus and Immotile Cilia;The American Journal of Human Genetics;1998-06