Genetics of the congenital absence of the vas deferens.
Bieth E, Hamdi SM, Mieusset R.
Hum Genet. 2021 Jan;140(1):59-76. doi: 10.1007/s00439-020-02122-w. Epub 2020 Feb 5.
Mutation analysis of the cystic fibrosis transmembrane conductance regulator gene in Chinese congenital absence of vas deferens patients.
Luo S, Feng J, Zhang Y, Yang X, Ma G, Hu T, Xi Y, Tu X, Wang C, Zhang H, Zou Z, Zhang Y.
Gene. 2021 Jan 10;765:145045. doi: 10.1016/j.gene.2020.145045. Epub 2020 Aug 8.
Common CFTR haplotypes and susceptibility to chronic pancreatitis and congenital bilateral absence of the vas deferens.
Steiner B, Rosendahl J, Witt H, Teich N, Keim V, Schulz HU, Pfützer R, Löhr M, Gress TM, Nickel R, Landt O, Koudova M, Macek M Jr, Farre A, Casals T, Desax MC, Gallati S, Gomez-Lira M, Audrezet MP, Férec C, des Georges M, Claustres M, Truninger K.
Hum Mutat. 2011 Aug;32(8):912-20. doi: 10.1002/humu.21511. Epub 2011 Jun 7.
Epididymal Appearance in Congenital Absence of Vas Deferens.
Gokhale S, Kochhar K.
J Ultrasound Med. 2021 Jun;40(6):1085-1090. doi: 10.1002/jum.15500. Epub 2020 Sep 21.
Congenital bilateral absence of the vas deferens as an atypical form of cystic fibrosis: reproductive implications and genetic counseling.
de Souza DAS, Faucz FR, Pereira-Ferrari L, Sotomaior VS, Raskin S.
Andrology. 2018 Jan;6(1):127-135. doi: 10.1111/andr.12450. Epub 2017 Dec 7.
The role of SLC9A3 in Taiwanese patients with congenital bilateral absence of vas deferens (CBAVD).
Chiang HS, Wang YY, Lin YH, Wu YN.
J Formos Med Assoc. 2019 Dec;118(12):1576-1583. doi: 10.1016/j.jfma.2019.01.019. Epub 2019 Feb 21.
Genetics of Azoospermia.
Cioppi F, Rosta V, Krausz C.
Int J Mol Sci. 2021 Mar 23;22(6):3264. doi: 10.3390/ijms22063264.
Congenital absence of vas deferens and ectopic kidney.
Salwan A, Abdelrahman A.
Int J Surg Case Rep. 2017;34:90-92. doi: 10.1016/j.ijscr.2017.03.019. Epub 2017 Mar 18.
CFTR variants and renal abnormalities in males with congenital unilateral absence of the vas deferens (CUAVD): a systematic review and meta-analysis of observational studies.
Cai H, Qing X, Niringiyumukiza JD, Zhan X, Mo D, Zhou Y, Shang X.
Genet Med. 2019 Apr;21(4):826-836. doi: 10.1038/s41436-018-0262-7. Epub 2018 Sep 14.
Diagnostics of CFTR-negative patients with congenital bilateral absence of vas deferens: which mutations are of most interest?
Ferlin A, Stuppia L.
Expert Rev Mol Diagn. 2020 Mar;20(3):265-267. doi: 10.1080/14737159.2020.1707081. Epub 2019 Dec 23.
