Recurrent Microdeletions at Xq27.3-Xq28 and Male Infertility: A Study in the Czech Population.

Chylíková, Blanka; Hrdlicka, Ivan; Veselá, Kamila; Rezábek, Karel; Liska, Frantisek

Chylíková, Blanka; Hrdlicka, Ivan; Veselá, Kamila; Rezábek, Karel; Liska, Frantisek.

Afiliação

Chylíková B; Institute of Biology and Medical Genetics, 1st Faculty of Medicine, Charles University in Prague and General University Hospital, Praha, Czech Republic.
Hrdlicka I; Institute of Biology and Medical Genetics, 1st Faculty of Medicine, Charles University in Prague and General University Hospital, Praha, Czech Republic.
Veselá K; Institute of Biology and Medical Genetics, 1st Faculty of Medicine, Charles University in Prague and General University Hospital, Praha, Czech Republic.
Rezábek K; Center for Assisted Reproduction, Clinic of Gynecology and Obstetrics, 1st Faculty of Medicine, Charles University in Prague and General University Hospital, Praha, Czech Republic.
Liska F; Institute of Biology and Medical Genetics, 1st Faculty of Medicine, Charles University in Prague and General University Hospital, Praha, Czech Republic.

PLoS One ; 11(6): e0156102, 2016.

Article em En | MEDLINE | ID: mdl-27257673

Assuntos

Deleção Cromossômica; Cromossomos Humanos X; Adulto; República Tcheca; Humanos; Infertilidade Masculina/genética; Masculino; Mutação; Fenótipo; Espermatozoides/patologia

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Deleção Cromossômica / Cromossomos Humanos X Tipo de estudo: Risk_factors_studies Limite: Adult / Humans / Male País/Região como assunto: Europa Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google