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A report on CF carrier frequency among men with infertility owing to congenital absence of the vas deferens.

作者信息

Williams C, Mayall E S, Williamson R, Hirsh A, Cookson H

出版信息

J Med Genet. 1993 Nov;30(11):973. doi: 10.1136/jmg.30.11.973-a.

DOI:10.1136/jmg.30.11.973-a
PMID:8301660
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1016620/
Abstract
摘要

相似文献

1
A report on CF carrier frequency among men with infertility owing to congenital absence of the vas deferens.关于因先天性输精管缺如导致不育的男性中囊性纤维化携带者频率的报告。
J Med Genet. 1993 Nov;30(11):973. doi: 10.1136/jmg.30.11.973-a.
2
[Congenital agenesis of the vas deferens and cystic fibrosis].[先天性输精管缺如与囊性纤维化]
Urologe A. 1995 Jul;34(4):348-50.
3
The incidence of cystic fibrosis gene mutations in patients with congenital bilateral absence of the vas deferens in Scotland.苏格兰先天性双侧输精管缺如患者中囊性纤维化基因突变的发生率。
Br J Urol. 1997 Jan;79(1):74-7. doi: 10.1046/j.1464-410x.1997.30816.x.
4
Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France.法国囊性纤维化和先天性输精管缺如中CFTR基因突变谱。
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5
Diagnostic criteria for cystic fibrosis in men with congenital absence of the vas deferens.
Medicine (Baltimore). 1995 Jan;74(1):42-7. doi: 10.1097/00005792-199501000-00004.
6
Genetic testing and counselling for congenital bilateral absence of the vas deferens.
Lancet. 1994 Jun 18;343(8912):1566-7. doi: 10.1016/s0140-6736(94)92964-5.
7
Congenital unilateral absence of the vas deferens: a heterogeneous disorder with two distinct subpopulations based upon aetiology and mutational status of the cystic fibrosis gene.
Hum Reprod. 1995 Jul;10(7):1728-35. doi: 10.1093/oxfordjournals.humrep.a136164.
8
Heterogeneous spectrum of mutations in CFTR gene from Indian patients with congenital absence of the vas deferens and their association with cystic fibrosis genetic modifiers.来自印度先天性输精管缺如患者的CFTR基因突变异质性谱及其与囊性纤维化遗传修饰因子的关联。
Mol Hum Reprod. 2014 Sep;20(9):827-35. doi: 10.1093/molehr/gau047. Epub 2014 Jun 23.
9
Cystic fibrosis in infertility: screening before assisted reproduction: opinion.
Hum Reprod. 2000 Nov;15(11):2415-7. doi: 10.1093/humrep/15.11.2415.
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Aetiology of congenital absence of vas deferens: genetic study of three generations.
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本文引用的文献

1
Vasa aplasia and cystic fibrosis.输精管发育不全与囊性纤维化。
Br J Urol. 1990 Nov;66(5):538-40. doi: 10.1111/j.1464-410x.1990.tb15006.x.
2
Abnormal distribution of CF delta F508 allele in azoospermic men with congenital aplasia of epididymis and vas deferens.先天性附睾和输精管发育不全的无精子症男性中CF ΔF508等位基因的异常分布。
Lancet. 1990 Aug 25;336(8713):512. doi: 10.1016/0140-6736(90)92066-q.
3
Analysis of 14 cystic fibrosis mutations in five south European populations.
Hum Genet. 1991 Oct;87(6):737-8. doi: 10.1007/BF00201737.
4
Influence of MHC and MHC-linked genes on reproduction.主要组织相容性复合体（MHC）及与MHC连锁的基因对生殖的影响。
Am J Hum Genet. 1992 Jan;50(1):1-5.
5
Congenital bilateral absence of the vas deferens. A primarily genital form of cystic fibrosis.先天性双侧输精管缺如。一种主要累及生殖系统的囊性纤维化类型。
JAMA. 1992 Apr 1;267(13):1794-7.
6
Cystic fibrosis genotypes and views on screening are both heterogeneous and population related.囊性纤维化的基因型以及关于筛查的观点既具有异质性又与人群相关。
Am J Hum Genet. 1992 Nov;51(5):943-50.