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https://hdl.handle.net/11499/5307
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Düzcan, Füsun | - |
dc.contributor.author | Atmaca, Münevver | - |
dc.contributor.author | Çetin, Gökhan Ozan | - |
dc.contributor.author | Bağcı, Hüseyin | - |
dc.date.accessioned | 2019-08-16T11:44:30Z | - |
dc.date.available | 2019-08-16T11:44:30Z | - |
dc.date.issued | 2003 | - |
dc.identifier.issn | 0001-6349 | - |
dc.identifier.uri | https://hdl.handle.net/11499/5307 | - |
dc.identifier.uri | https://doi.org/10.1034/j.1600-0412.2003.820109.x | - |
dc.description.abstract | Background. Cytogenetic studies in patients with reproductive failure Aim. To investigate the contribution of chromosomal abnormalities in sub fertility and in couples with repeated abortions. Methods. Hundred and 13 couples who had at least two or more spontaneous abortions and 65 women and 63 men with infertility were analyzed cytogenetically. Results. Major chromosomal rearrangements were found in 8% and minor variants in 6% in the study population. Major chromosomal aberrations were judged to explain 4.9% of recurrent abortions and 13% of infertility. Chromosomal abnormalities in infertile men occurred in 5% and in infertile women in 21.5%. The chromosomal abnormalities were structural (57%), numerical (18%) or mosaics (25%). Conclusions. Chromosomal aberrations in recurrent abortions are mostly structural ones and those in female infertility mosaicism of sex chromosomes. Turner's syndrome, Turner variants and XY females are detected as a cause of female infertility. The structural and numerical aberrations of either sex or autosomal chromosomes were found in infertile men. | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | Acta Obstetricia et Gynecologica Scandinavica | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Chromosomal abnormalities | en_US |
dc.subject | Infertility | en_US |
dc.subject | Recurrent abortion | en_US |
dc.subject | Reproductive failure | en_US |
dc.subject | article | en_US |
dc.subject | autosomal disorder | en_US |
dc.subject | chromosome aberration | en_US |
dc.subject | chromosome analysis | en_US |
dc.subject | chromosome mosaicism | en_US |
dc.subject | chromosome number | en_US |
dc.subject | chromosome structure | en_US |
dc.subject | chromosome variant | en_US |
dc.subject | controlled study | en_US |
dc.subject | cytogenetics | en_US |
dc.subject | female | en_US |
dc.subject | female infertility | en_US |
dc.subject | human | en_US |
dc.subject | karyotype | en_US |
dc.subject | karyotype 46,XY | en_US |
dc.subject | major clinical study | en_US |
dc.subject | male | en_US |
dc.subject | male infertility | en_US |
dc.subject | numerical chromosome aberration | en_US |
dc.subject | population research | en_US |
dc.subject | priority journal | en_US |
dc.subject | recurrent abortion | en_US |
dc.subject | reproductive health | en_US |
dc.subject | sex chromosome | en_US |
dc.subject | structural chromosome aberration | en_US |
dc.subject | subfertility | en_US |
dc.subject | Turner syndrome | en_US |
dc.subject | Abortion, Spontaneous | en_US |
dc.subject | Chromosome Aberrations | en_US |
dc.subject | Chromosome Banding | en_US |
dc.subject | Chromosome Disorders | en_US |
dc.subject | Chromosomes, Human, 1-3 | en_US |
dc.subject | Chromosomes, Human, 6-12 and X | en_US |
dc.subject | Chromosomes, Human, Y | en_US |
dc.subject | Female | en_US |
dc.subject | Gene Rearrangement | en_US |
dc.subject | Humans | en_US |
dc.subject | Infertility, Female | en_US |
dc.subject | Infertility, Male | en_US |
dc.subject | Inversion, Chromosome | en_US |
dc.subject | Karyotyping | en_US |
dc.subject | Male | en_US |
dc.subject | Polymorphism, Genetic | en_US |
dc.title | Cytogenetic studies in patients with reproductive failure | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 82 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.startpage | 53 | - |
dc.identifier.startpage | 53 | en_US |
dc.identifier.endpage | 56 | en_US |
dc.identifier.doi | 10.1034/j.1600-0412.2003.820109.x | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.pmid | 12580840 | en_US |
dc.identifier.scopus | 2-s2.0-0037285745 | en_US |
dc.identifier.wos | WOS:000180967200009 | en_US |
dc.identifier.scopusquality | Q1 | - |
dc.owner | Pamukkale_University | - |
item.fulltext | No Fulltext | - |
item.languageiso639-1 | en | - |
item.grantfulltext | none | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.openairetype | Article | - |
item.cerifentitytype | Publications | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 01. Pamukkale University | - |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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