A rare combination of 45,X/46,XY mosaicism and Y chromosome microdeletion in an infertile man with azoospermia
dc.contributor.author | Aydemir, Hüseyin | |
dc.contributor.author | Karkucak, Mutlu | |
dc.contributor.author | Cimen, Hacı İbrahim | |
dc.contributor.author | Halis, Fikret | |
dc.contributor.author | Kumsar, Şükrü | |
dc.contributor.author | Sonbahar, Adil E. | |
dc.contributor.buuauthor | Yakut, Tahsin | |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi//Tıbbi Genetik Anabilim Dalı. | tr_TR |
dc.contributor.scopusid | 6602802424 | tr_TR |
dc.date.accessioned | 2023-06-07T12:24:16Z | |
dc.date.available | 2023-06-07T12:24:16Z | |
dc.date.issued | 2016 | |
dc.identifier.citation | Aydemir, H. vd. (2016). "A rare combination of 45,X/46,XY mosaicism and Y chromosome microdeletion in an infertile man with azoospermia". Genetic Counseling, 27(1), 95-98. | en_US |
dc.identifier.endpage | 98 | tr_TR |
dc.identifier.issn | 1015-8146 | |
dc.identifier.issue | 1 | tr_TR |
dc.identifier.pubmed | 27192898 | tr_TR |
dc.identifier.scopus | 2-s2.0-85001740534 | tr_TR |
dc.identifier.startpage | 95 | tr_TR |
dc.identifier.uri | http://hdl.handle.net/11452/32963 | |
dc.identifier.volume | 27 | tr_TR |
dc.identifier.wos | 000385210500012 | tr_TR |
dc.indexed.pubmed | PubMed | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.wos | SCIE | en_US |
dc.language.iso | en | en_US |
dc.publisher | Medecine et Hygiene | en_US |
dc.relation.collaboration | Yurt içi | tr_TR |
dc.relation.journal | Genetic Counseling | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.rights | info:eu-repo/semantics/closedAccess | tr_TR |
dc.subject | Biotechnology & applied microbiology | en_US |
dc.subject | Genetics & heredity | en_US |
dc.subject | Medical ethics | en_US |
dc.subject | Research & experimental medicine | en_US |
dc.subject | Deletions | en_US |
dc.subject.emtree | 45,X/46,XY mosaicism | en_US |
dc.subject.emtree | Adult | en_US |
dc.subject.emtree | Azoospermia | en_US |
dc.subject.emtree | Blood sampling | en_US |
dc.subject.emtree | Case report | en_US |
dc.subject.emtree | Centromere | en_US |
dc.subject.emtree | Chromosome analysis | en_US |
dc.subject.emtree | Chromosome deletion Y | en_US |
dc.subject.emtree | Clinical article | en_US |
dc.subject.emtree | DNA isolation | en_US |
dc.subject.emtree | Doppler ultrasonography | en_US |
dc.subject.emtree | Echocardiography | en_US |
dc.subject.emtree | Genetic variation | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Karyotype | en_US |
dc.subject.emtree | Letter | en_US |
dc.subject.emtree | Male | en_US |
dc.subject.emtree | Male infertility | en_US |
dc.subject.emtree | Multiplex polymerase chain reaction | en_US |
dc.subject.emtree | Phenotype | en_US |
dc.subject.emtree | Semen analysis | en_US |
dc.subject.emtree | X chromosome | en_US |
dc.subject.emtree | Y chromosome | en_US |
dc.subject.emtree | Y chromosome microdeletion | en_US |
dc.subject.emtree | Azoospermia | en_US |
dc.subject.emtree | Chromosome deletion | en_US |
dc.subject.emtree | Disorder of sex development | en_US |
dc.subject.emtree | Genetics | en_US |
dc.subject.emtree | Mosaicism | en_US |
dc.subject.emtree | Sex chromosome aberration | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Azoospermia | en_US |
dc.subject.mesh | Chromosome deletion | en_US |
dc.subject.mesh | Chromosomes, human, Y | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Mosaicism | en_US |
dc.subject.mesh | Sex chromosome aberrations | en_US |
dc.subject.mesh | Sex chromosome disorders of sex development | en_US |
dc.subject.wos | Biotechnology & applied microbiology | en_US |
dc.subject.wos | Genetics & heredity | en_US |
dc.subject.wos | Medical ethics | en_US |
dc.subject.wos | Medicine, research & experimental | en_US |
dc.title | A rare combination of 45,X/46,XY mosaicism and Y chromosome microdeletion in an infertile man with azoospermia | en_US |
dc.type | Letter |
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