Carriage of cystic fibrosis mutation through the prism of ART (the current state of the problem)


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Abstract

Cystic fibrosis is one of the most common monogenic diseases in the European population. The paper considers the possibilities of current reproductive technologies to prevent the inheritance of the cystic fibrosis gene in the children of patients with different types of monogenic disease.

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About the authors

K. Krasnopolskaya

Moscow Regional Research Institute of Obstetrics and Gynecology

Professor

I. Shuginin

Moscow Regional Research Institute of Obstetrics and Gynecology

N. Sesina

Semiya (Family) International Clinic

Email: sesina@maii.ru

E. Voskoboeva

Medical Genetic Research Center; Genlab Clinical and Diagnostic Laboratory of Human Reproduction

A. Beketova

Moscow Regional Research Institute of Obstetrics and Gynecology

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