PubMed

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

Radpour R, Taherzadeh-Fard E, Gourabi H, Aslani S, Vosough Dizaj A, Aslani A.

Reprod Biomed Online. 2009 Mar;18(3):327-32.PMID: 19298730 [PubMed - indexed for MEDLINE]Related articles

Heterogenous spectrum of CFTR gene mutations in Indian patients with congenital absence of vas deferens.

Sharma N, Acharya N, Singh SK, Singh M, Sharma U, Prasad R.

Hum Reprod. 2009 May;24(5):1229-36. Epub 2009 Jan 30.PMID: 19181743 [PubMed - indexed for MEDLINE]Related articles

Gene copy number variations in Asian patients with congenital bilateral absence of the vas deferens.

Lee CH, Wu CC, Wu YN, Chiang HS.

Hum Reprod. 2009 Mar;24(3):748-55. Epub 2008 Dec 17.PMID: 19095672 [PubMed - indexed for MEDLINE]Related articles

CFTR mutation analysis of a Caucasian father with congenital bilateral absence of vas deferens, a Taiwanese mother, and twins resulting from ICSI procedure.

Chiang HS, Wu CC, Wu YN, Lu JF, Lin GH, Hwang JL.

J Formos Med Assoc. 2008 Sep;107(9):736-40.PMID: 18796364 [PubMed - indexed for MEDLINE]Related articlesFree article

Activated caspases in thawed epididymal and testicular spermatozoa of patients with congenital bilateral absence of the vas deferens and intracytoplasmic sperm injection outcome.

Brugnon F, Janny L, Artonne C, Sion B, Pouly JL, Grizard G.

Fertil Steril. 2009 Aug;92(2):557-64. Epub 2008 Sep 6.PMID: 18774565 [PubMed - indexed for MEDLINE]Related articles

Molecular and functional characterization of CBAVD-causing mutations located in CFTR nucleotide-binding domains.

Grangeia A, Barro-Soria R, Carvalho F, Damas AM, Maurício AC, Kunzelmann K, Barros A, Sousa M.

Cell Physiol Biochem. 2008;22(1-4):79-92. Epub 2008 Jul 25.PMID: 18769034 [PubMed - indexed for MEDLINE]Related articles

Multiplex allele-specific fluorescent PCR for haplotyping the IVS8 (TG)m(T)n locus in the CFTR gene.

Costa C, Costa JM, Martin J, Boissier B, Goossens M, Girodon E.

Clin Chem. 2008 Sep;54(9):1564-7.PMID: 18755906 [PubMed - indexed for MEDLINE]Related articlesFree article

Genetic investigations of CFTR mutations in congenital absence of vas deferens, uterus, and vagina as a cause of infertility.

Radpour R, Gourabi H, Dizaj AV, Holzgreve W, Zhong XY.

J Androl. 2008 Sep-Oct;29(5):506-13. Epub 2008 Jun 20. Review.PMID: 18567645 [PubMed - indexed for MEDLINE]Related articlesFree article

Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutation associated with a congenital bilateral absence of vas deferens.

Sakamoto H, Yajima T, Suzuki K, Ogawa Y.

Int J Urol. 2008 Mar;15(3):270-1.PMID: 18304229 [PubMed - indexed for MEDLINE]Related articles

Infertility and its management in men with cystic fibrosis: review of literature and clinical practices in the UK.

Popli K, Stewart J.

Hum Fertil (Camb). 2007 Dec;10(4):217-21. Review.PMID: 18049957 [PubMed - indexed for MEDLINE]Related articles

Novel CFTR missense mutations in Brazilian patients with congenital absence of vas deferens: counseling issues.

Pieri Pde C, Missaglia MT, Roque Jde A, Moreira-Filho CA, Hallak J.

Clinics (Sao Paulo). 2007 Aug;62(4):385-90.PMID: 17823699 [PubMed - indexed for MEDLINE]Related articlesFree article

Correlation between CFTR gene mutations in Iranian men with congenital absence of the vas deferens and anatomical genital phenotype.

Radpour R, Gourabi H, Gilani MA, Dizaj AV.

J Androl. 2008 Jan-Feb;29(1):35-40. Epub 2007 Aug 1.PMID: 17673436 [PubMed - indexed for MEDLINE]Related articlesFree article

Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations.

Alibakhshi R, Kianishirazi R, Cassiman JJ, Zamani M, Cuppens H.

J Cyst Fibros. 2008 Mar;7(2):102-9. Epub 2007 Jul 27.PMID: 17662673 [PubMed - indexed for MEDLINE]Related articles

Three singleton deliveries with healthy children from one couple after cryo-tESE and ICSI.

Schmutzler AG, Glander M, Acar B, Chanysheva O, Buck S, Martinez Portillo FJ, Mettler L.

Clin Exp Obstet Gynecol. 2007;34(2):106-8.PMID: 17629165 [PubMed - indexed for MEDLINE]Related articles

Cystic fibrosis transmembrane conductance regulator is vital to sperm fertilizing capacity and male fertility.

Xu WM, Shi QX, Chen WY, Zhou CX, Ni Y, Rowlands DK, Yi Liu G, Zhu H, Ma ZG, Wang XF, Chen ZH, Zhou SC, Dong HS, Zhang XH, Chung YW, Yuan YY, Yang WX, Chan HC.

Proc Natl Acad Sci U S A. 2007 Jun 5;104(23):9816-21. Epub 2007 May 22.PMID: 17519339 [PubMed - indexed for MEDLINE]Related articlesFree article

Large genomic rearrangements in the CFTR gene contribute to CBAVD.

Taulan M, Girardet A, Guittard C, Altieri JP, Templin C, Beroud C, des Georges M, Claustres M.

BMC Med Genet. 2007 Apr 20;8:22.PMID: 17448246 [PubMed - indexed for MEDLINE]Related articlesFree article

Novel CFTR gene mutation in a patient with CBAVD.

Goh DL, Zhou Y, Chong SS, Ngiam NS, Goh DY.

J Cyst Fibros. 2007 Nov 30;6(6):423-5. Epub 2007 Mar 29.PMID: 17398169 [PubMed - indexed for MEDLINE]Related articles

Variable penetrance and expressivity of the splice altering 5T sequence in the cystic fibrosis gene.

Lebo RV, Grody WW.

Genet Test. 2007 Spring;11(1):32-44.PMID: 17394391 [PubMed - indexed for MEDLINE]Related articles

Detection of cystic fibrosis transmembrane conductance regulator (CFTR) gene rearrangements enriches the mutation spectrum in congenital bilateral absence of the vas deferens and impacts on genetic counselling.

Ratbi I, Legendre M, Niel F, Martin J, Soufir JC, Izard V, Costes B, Costa C, Goossens M, Girodon E.

Hum Reprod. 2007 May;22(5):1285-91. Epub 2007 Feb 28.PMID: 17329263 [PubMed - indexed for MEDLINE]Related articlesFree article

Molecular study of (TG)m(T)n polymorphisms in Iranian males with congenital bilateral absence of the vas deferens.

Radpour R, Gourabi H, Gilani MA, Dizaj AV.

J Androl. 2007 Jul-Aug;28(4):541-7. Epub 2007 Feb 21.PMID: 17314234 [PubMed - indexed for MEDLINE]Related articlesFree article