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

Open Access

Peer-reviewed

Research Article

Blanka Chylíková,

Affiliation Institute of Biology and Medical Genetics, 1st Faculty of Medicine, Charles University in Prague and General University Hospital, Praha, Czech Republic
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Ivan Hrdlička,

Affiliation Institute of Biology and Medical Genetics, 1st Faculty of Medicine, Charles University in Prague and General University Hospital, Praha, Czech Republic
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Kamila Veselá,

Affiliation Institute of Biology and Medical Genetics, 1st Faculty of Medicine, Charles University in Prague and General University Hospital, Praha, Czech Republic
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Karel Řežábek,

Affiliation Center for Assisted Reproduction, Clinic of Gynecology and Obstetrics, 1st Faculty of Medicine, Charles University in Prague and General University Hospital, Praha, Czech Republic
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František Liška

* E-mail: frantisek.liska@lf1.cuni.cz

Affiliation Institute of Biology and Medical Genetics, 1st Faculty of Medicine, Charles University in Prague and General University Hospital, Praha, Czech Republic
⨯

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Male infertility
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Sperm
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X chromosomes
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Semen
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Human genetics
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Polymerase chain reaction
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Chromosomal deletions
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