Molecular Screening of theCFTRGene in Mexican Patients with Congenital Absence of the Vas Deferens-Reference-Cited by-同舟云学术

Molecular Screening of theCFTRGene in Mexican Patients with Congenital Absence of the Vas Deferens

Published:2012-04 Issue:4 Volume:16 Page:292-296
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Saldaña-Alvarez Yolanda¹²,Jiménez-Morales Silvia¹,Echevarría-Sánchez Mirna³,Jiménez-Ruíz Juan Luis¹,García-Cavazos Ricardo⁴,Velázquez-Cruz Rafael¹,Carnevale Alessandra¹,Orozco Lorena¹⁵

Affiliation:

1. Genomic of Complex Diseases Laboratoy, Instituto Nacional de Medicina Genómica, SS, Mexico City, Mexico.

2. Programa Institucional de Biomedicina Molecular, ENMyH-IPN, Mexico City, Mexico.

3. Department of Andrology, Instituto Nacional de Perinatología, Mexico City, Mexico.

4. Subsecretaría de Salud del Distrito Federal, Mexico City, Mexico.

5. Genomics Sciences Program, Universidad Autónoma de la Cd. de México, Mexico City, Mexico.

Publisher

Mary Ann Liebert Inc

Subject

Genetics (clinical),General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/gtmb.2011.0124

Reference37 articles.

1. CFTR (TG)m(T)n polymorphism in patients with CBAVD in a population expressing low incidence of cystic fibrosis

2. Mutations in the Cystic Fibrosis Gene in Patients with Congenital Absence of the Vas Deferens

3. Genetic basis of variable exon 9 skipping in cystic fibrosis transmembrane conductance regulator mRNA

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

5. Improved detection of cystic fibrosis mutations in infertility patients with DNA sequence analysis

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1. CFTR gene variants as a reason for impaired spermatogenesis: a pilot study and a Meta-analysis of published data;Human Fertility;2021-03-15

2. Congenital absence of the vas deferens: Cystic fibrosis transmembrane regulatory gene mutations;Best Practice & Research Clinical Endocrinology & Metabolism;2020-12

3. Congenital bilateral absence of the vas deferens as an atypical form of cystic fibrosis: reproductive implications and genetic counseling;Andrology;2017-12-07