Characterization of gene mutations and phenotypes of cystic fibrosis in Chinese patients

Different Cystic Fibrosis Transmembrane Conductance Regulator Mutations in Chinese Men With Congenital Bilateral Absence of Vas Deferens and Other Acquired Obstructive Azoospermia

(2013) Shaoming Lu et al.   UROLOGY

Personalized Medicine in Cystic Fibrosis

(2012) John P. Clancy et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

The CFTR polymorphisms poly-T, TG-repeats and M470V in Chinese males with congenital bilateral absence of the vas deferens

(2012) Wu-Hua Ni et al.   ASIAN JOURNAL OF ANDROLOGY

Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) in Chinese patients with congenital bilateral absence of vas deferens

(2012) Hongjun Li et al.   Journal of Cystic Fibrosis

Comparing the American and European diagnostic guidelines for cystic fibrosis: same disease, different language?

(2012) Chee Y Ooi et al.   THORAX

Allergic Bronchopulmonary Aspergillosis in Asthma and Cystic Fibrosis

(2011) Alan P. Knutsen et al.   Clinical & Developmental Immunology

CFTR mutations in men with congenital bilateral absence of the vas deferens (CBAVD): a systemic review and meta-analysis

(2011) Jianmin Yu et al.   HUMAN REPRODUCTION

Recommendations for the classification of diseases as CFTR-related disorders

(2011) C. Bombieri et al.   Journal of Cystic Fibrosis

Heterogeneous Spectrum of CFTR Gene Mutations in Korean Patients with Cystic Fibrosis

(2011) Haiyoung Jung et al.   Korean Journal of Laboratory Medicine

Skipping of exon 12 as a consequence of a point mutation (1898 + 5G → T) in the cystic fibrosis transmembrane conductance regulator gene found in a consanguineous Chinese family

(2010) Julian Zielenski et al.   CLINICAL GENETICS

Guidelines for Diagnosis of Cystic Fibrosis in Newborns through Older Adults: Cystic Fibrosis Foundation Consensus Report

(2008) Philip M. Farrell et al.   JOURNAL OF PEDIATRICS