(Q39022376)

8 September 2017

title

Screening of ΔF508 mutation and IVS8-poly T polymorphism in CFTR gene in Tunisian infertile men without CBAVD. (English)

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8 September 2017

M Ghorbel

1

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8 September 2017

S Baklouti-Gargouri

2

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8 September 2017

R Keskes

3

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8 September 2017

A Sellami-Ben Hamida

4

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8 September 2017

N Feki-Chakroun

5

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8 September 2017

A Bahloul

6

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8 September 2017

F Fakhfakh

7

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8 September 2017

L Ammar-Keskes

8

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8 September 2017

publication date

18 July 2011

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8 September 2017

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8 September 2017

volume

44 Suppl 1

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8 September 2017

page(s)

376-382

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Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens.

8 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1439-0272.2011.01193.X

Genetic diagnosis in infertile men with numerical and constitutional sperm abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1439-0272.2011.01193.X

Mutations of the CFTR gene in Turkish patients with congenital bilateral absence of the vas deferens.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1439-0272.2011.01193.X

Y chromosome microdeletions and alterations of spermatogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1439-0272.2011.01193.X

Detection of sperm in men with Y chromosome microdeletions of the AZFa, AZFb and AZFc regions

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1439-0272.2011.01193.X

CFTR is essential for sperm fertilizing capacity and is correlated with sperm quality in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1439-0272.2011.01193.X

Rational approach to genetic testing of cystic fibrosis (CF) in infertile men.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1439-0272.2011.01193.X

Substantial prevalence of microdeletions of the Y-chromosome in infertile men with idiopathic azoospermia and oligozoospermia detected using a sequence-tagged site-based mapping strategy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1439-0272.2011.01193.X

Relevance of genetic counselling in couples prior to intracytoplasmic sperm injection.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1439-0272.2011.01193.X

Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1439-0272.2011.01193.X

Y chromosome microdeletions in Tunisian infertile males

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1439-0272.2011.01193.X

Increased frequency of cystic fibrosis transmembrane conductance regulator gene mutations in infertile males

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1439-0272.2011.01193.X

CFTR gene mutations and male infertility.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1439-0272.2011.01193.X

Combined cytogenetic and Y chromosome microdeletion screening in males undergoing intracytoplasmic sperm injection.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1439-0272.2011.01193.X

Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1439-0272.2011.01193.X

Heterogeneity for mutations in the CFTR gene and clinical correlations in patients with congenital absence of the vas deferens

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1439-0272.2011.01193.X

10.1111/J.1439-0272.2011.01193.X

21 January 2018

Identifiers

DOI

1 reference

8 September 2017

1 reference