Molecular screening of CFTR gene in Egyptian patients with congenital bilateral absence of the vas deferens: a preliminary study.

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CFTR Gene Mutations in the Egyptian Population: Current and Future Insights for Genetic Screening Strategy.The CFTR gene mild variants poly-T, TG repeats and M470V detection in Indian men with congenital bilateral absence of vas deferens.

P2860

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Molecular screening of CFTR gene in Egyptian patients with congenital bilateral absence of the vas deferens: a preliminary study.

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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2016年论文

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2016年论文

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name

Molecular screening of CFTR ge ...... deferens: a preliminary study.

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Molecular screening of CFTR ge ...... deferens: a preliminary study.

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Molecular screening of CFTR ge ...... deferens: a preliminary study.

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Molecular screening of CFTR ge ...... deferens: a preliminary study.

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Molecular screening of CFTR ge ...... deferens: a preliminary study.

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Molecular screening of CFTR ge ...... deferens: a preliminary study.

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P1476

Molecular screening of CFTR ge ...... deferens: a preliminary study.

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P2093

A Zeidan

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D A Mehaney

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F A Hassan

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M Amer

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M Fathy

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T Ramzy

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P2860

Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders--updated European recommendations

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

CFTR mutations in men with congenital bilateral absence of the vas deferens (CBAVD): a systemic review and meta-analysis.

Clinical, laboratory and genetic assessment of patients with congenital bilateral absent vas deferens.

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.

Cystic fibrosis detection in high-risk Egyptian children and CFTR mutation analysis.

Profile of cystic fibrosis in a single referral center in Egypt

The CFTR polymorphisms poly-T, TG-repeats and M470V in Chinese males with congenital bilateral absence of the vas deferens.

Ivacaftor potentiation of multiple CFTR channels with gating mutations.

CFTR gene mutations in Japanese individuals with congenital bilateral absence of the vas deferens.

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scholarly article

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10.1111/AND.12563

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Mohamed A. Elmonem

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2016-03-15T00:00:00Z

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295079181

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P921

birth defect

Molecular screening of CFTR gene in Egyptian patients with congenital bilateral absence of the vas deferens: a preliminary study.

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P2860

P2860

Molecular screening of CFTR gene in Egyptian patients with congenital bilateral absence of the vas deferens: a preliminary study.

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type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P921

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P921