Congenital bilateral absence of the vas deferens as an atypical form of cystic fibrosis: reproductive implications and genetic counseling

Benign outcome among positive cystic fibrosis newborn screen children with non-CF-causing variants

(2015) Danieli Barino Salinas et al.   Journal of Cystic Fibrosis

Association of cystic fibrosis transmembrane-conductance regulator gene mutation with negative outcome of intracytoplasmic sperm injection pregnancy in cases of congenital bilateral absence of vas deferens

(2014) Shaoming Lu et al.   FERTILITY AND STERILITY

Congenital absence of the vas deferens and unilateral renal agenesis: implications for patient and family

(2014) Victoria Alison Lane et al.   PEDIATRIC SURGERY INTERNATIONAL

CFTR p.Arg117His associated with CBAVD and other CFTR-related disorders

(2013) Christel Thauvin-Robinet et al.   JOURNAL OF MEDICAL GENETICS

Next generation diagnostics of cystic fibrosis andCFTR-related disorders by targeted multiplex high-coverage resequencing ofCFTR

(2013) D Trujillano et al.   JOURNAL OF MEDICAL GENETICS

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

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

Regulation of male fertility by CFTR and implications in male infertility

(2012) Hui Chen et al.   HUMAN REPRODUCTION UPDATE

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

Cystic fibrosis transmembrane conductance regulator mutations and polymorphisms associated with congenital bilateral absence of vas deferens in a restricted group of patients from North Africa

(2011) M. Boudaya et al.   ANNALS OF HUMAN BIOLOGY

Enhanced frequency of CFTR gene variants in couples who are candidates for assisted reproductive technology treatment

(2011) Rossella Tomaiuolo et al.   CLINICAL CHEMISTRY AND LABORATORY MEDICINE

Mutation Studies in the CFTR Gene in Asian Indian Subjects with Congenital Bilateral Absence of Vas Deferens: Report of Two Novel Mutations and Four Novel Variants

(2011) Kabir Sachdeva et al.   Genetic Testing and Molecular Biomarkers

Molecular Screening of the CFTR Gene in Mexican Patients with Congenital Absence of the Vas Deferens

(2011) Yolanda Saldaña-Alvarez et al.   Genetic Testing and Molecular Biomarkers

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

The D1152H cystic fibrosis mutation in prenatal carrier screening, patients and prenatal diagnosis

(2011) Leah Peleg et al.   JOURNAL OF MEDICAL SCREENING

Link between CFTR mutations and ABPA: a systematic review and meta-analysis

(2011) Ritesh Agarwal et al.   MYCOSES

Cystic Fibrosis Transmembrane Conductance Regulator Channel Dysfunction in Non–Cystic Fibrosis Bronchiectasis

(2010) Thierry Bienvenu et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Clinical, laboratory and genetic assessment of patients with congenital bilateral absent vas deferens

(2010) T. M. Hussein et al.   ANDROLOGIA

Mutations of the cystic fibrosis gene in patients with bronchiectasis associated with rheumatoid arthritis

(2010) X. Puechal et al.   ANNALS OF THE RHEUMATIC DISEASES

Identification of the second CFTR mutation in patients with congenital bilateral absence of vas deferens undergoing ART protocols

(2010) Rossella Giuliani et al.   ASIAN JOURNAL OF ANDROLOGY

Congenital bilateral absence of vas deferens with a new missense mutation (P499A) in the CFTR gene

(2010) C. Arduino et al.   CLINICAL GENETICS

Association of cystic fibrosis genetic modifiers with congenital bilateral absence of the vas deferens

(2010) Viktoria Havasi et al.   FERTILITY AND STERILITY

Does the outcome of ICSI in cases of obstructive azoospermia depend on the origin of the retrieved spermatozoa or the cause of obstruction? A comparative analysis

(2010) Ahmed Kamal et al.   FERTILITY AND STERILITY

Independent Contribution of Common CFTR Variants to Chronic Pancreatitis

(2010) Rafael de Cid et al.   PANCREAS

Novel cause of hereditary obstructive azoospermia: a T2 allele in the CFTR gene

(2010) Ramin Radpour et al.   REPRODUCTIVE BIOMEDICINE ONLINE

Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients

(2007) Salmo Raskin et al.   Journal of Cystic Fibrosis