Congenital bilateral absence of the vas deferens: clinical characteristics, biological parameters, cystic fibrosis transmembrane conductance regulator gene mutations, and implications for genetic counseling (Q73303581)

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scientific article published on 01 December 2000

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English	Congenital bilateral absence of the vas deferens: clinical characteristics, biological parameters, cystic fibrosis transmembrane conductance regulator gene mutations, and implications for genetic counseling	scientific article published on 01 December 2000

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scholarly article

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2 November 2019

Congenital bilateral absence of the vas deferens: clinical characteristics, biological parameters, cystic fibrosis transmembrane conductance regulator gene mutations, and implications for genetic counseling (English)

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Europe PubMed Central

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2 November 2019

cystic fibrosis

1 reference

based on heuristic

inferred from title

congenital bilateral aplasia of the vas deferens

1 reference

based on heuristic

inferred from title

3

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2 November 2019

6

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2 November 2019

author name string

M Daudin

1

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2 November 2019

E Bieth

2

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2 November 2019

G Massat

4

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2 November 2019

F Pontonnier

5

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2 November 2019

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publication date

1 December 2000

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2 November 2019

Fertility and Sterility

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2 November 2019

74

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2 November 2019

6

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2 November 2019

1164-1174

1 reference

Europe PubMed Central

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2 November 2019

Abnormal distribution of CF delta F508 allele in azoospermic men with congenital aplasia of epididymis and vas deferens

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Congenital bilateral absence of the vas deferens. A primarily genital form of cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Aetiology of congenital absence of vas deferens: genetic study of three generations

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Congenital bilateral absence of vas deferens in the absence of cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Congenital bilateral absence of the vas deferens (CBAVD) and cystic fibrosis transmembrane regulator (CFTR): correlation between genotype and phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Correlation between genito-urinary anomalies, semen analysis and CFTR genotype in patients with congenital bilateral absence of the vas deferens

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Proportion of cystic fibrosis gene mutations not detected by routine testing in men with obstructive azoospermia

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Mutations in the cystic fibrosis gene in men with congenital bilateral absence of the vas deferens

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Genotype and phenotype in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

The spectrum of cystic fibrosis mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Frequent occurrence of the CFTR intron 8 (TG)n 5T allele in men with congenital bilateral absence of the vas deferens

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Congenital absence of the vas deferens: incomplete penetrance of cystic fibrosis gene mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Heterogeneity of reproductive tract abnormalities in men with absence of the vas deferens: role of cystic fibrosis transmembrane conductance regulator gene mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Cystic fibrosis mutation screening in healthy men with reduced sperm quality

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Increased levels of serum follicle-stimulating hormone and luteinizing hormone associated with intrinsic testicular hyperthermia in oligospermic infertile men

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Testicular size in infertile men: relationship to semen characteristics and hormonal blood levels

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Identification of mutations in exons 1 through 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

The search for south European cystic fibrosis mutations: identification of two new mutations, four variants, and intronic sequences.

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Molecular characterization of cystic fibrosis: 16 novel mutations identified by analysis of the whole cystic fibrosis conductance transmembrane regulator (CFTR) coding regions and splice site junctions

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

The complex relationships between cystic fibrosis and congenital bilateral absence of the vas deferens: clinical, electrophysiological and genetic data

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Autosomal recessive hereditary congenital aplasia of the vasa deferentia in four siblings.

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Molecular analysis of the cystic fibrosis gene reveals a high frequency of the intron 8 splice variant 5T in Egyptian males with congenital bilateral absence of the vas deferens

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Extensive analysis of 40 infertile patients with congenital absence of the vas deferens: in 50% of cases only one CFTR allele could be detected

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Aetiology of testicular cancer: association with congenital abnormalities, age at puberty, infertility, and exercise. United Kingdom Testicular Cancer Study Group

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Men with congenital absence of the vas deferens often have seminal vesicles

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

The vas deferens in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Congenital mesonephric defects in male infants with mucoviscidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

The diagnosis of cystic fibrosis: a consensus statement. Cystic Fibrosis Foundation Consensus Panel

1 reference

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7 January 2021

Screening practices for mutations in the CFTR gene ABCC7.

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2800%2901625-3

7 January 2021

Identifiers

10.1016/S0015-0282(00)01625-3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11119745%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11119745%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

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