Case report: Novel cause of hereditary obstructive azoospermia: a T2 allele in the CFTR gene

Author： Radpour Ramin   Taherzadeh-Fard Elahe   Gourabi Hamid   Aslani Sahar   Vosough Dizaj Ahmad   Aslani Ali  

Publisher： Reproductive Healthcare Ltd

ISSN： 1472-6483

Source： Reproductive BioMedicine Online, Vol.18, Iss.3, 2009-03, pp. : 327-332

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Molecular analysis of mutations and polymorphisms in the CFTR gene in male infertility

By Tamburino L   Guglielmino A   Venti E   Chamayou S  

Reproductive BioMedicine Online, Vol. 17, Iss. 1, 2008-07 ,pp. : 27-35

Reproductive Healthcare Ltd

Access to resources Recommend Favorite

The CYP2D6 gene locus in South African Coloureds: unique allele distributions, novel alleles and gene arrangements

By Gaedigk Andrea  

European Journal of Clinical Pharmacology, Vol. 64, Iss. 5, 2008-05 ,pp. : 465-475

Springer Publishing Company

Access to resources Recommend Favorite

Finasteride: Azoospermia: case report

By  

Reactions Weekly, Vol. 1, Iss. 1348-1349, 2011-01 ,pp. : 19-19

Adis International

Access to resources Recommend Favorite

Testosterone: Azoospermia: case report

By  

Reactions Weekly, Vol. 1, Iss. 1413, 2012-01 ,pp. : 42-42

Adis International

Access to resources Recommend Favorite

Sirolimus: Azoospermia: case report

By  

Reactions Weekly, Vol. 1, Iss. 1175, 2007-01 ,pp. : 23-23

Adis International

Access to resources Recommend Favorite