Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/24910
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dc.contributor.authorTatar, Abdulgani-
dc.contributor.authorÖztaş, Sıtkı-
dc.contributor.authorÖrs, Rahmi-
dc.date.accessioned2022-03-08T11:02:02Z-
dc.date.available2022-03-08T11:02:02Z-
dc.date.issued2005-
dc.identifier.citationTatar, A. vd. (2005). "A dysmorphic newborn with 45,X,der(1)inv(1)(p13;qter)t(Y;1)(pter -> 4q11;p13),-Y De novo karyotype". Genetic Counseling, 16(2), 173-177.en_US
dc.identifier.issn1015-8146-
dc.identifier.urihttp://hdl.handle.net/11452/24910-
dc.description.abstractA dysmorphic newborn with 45,x,der(1)inv,(1)(p13;qter)t(y;1)(pter -> q11;p13),-Y de novo karyotype: Y/autosome translocations are very rare chromosomal rearrangements. In most cases, the long arm of the Y chromosome is translocated onto an autosome and most patients are referred because of male infertility. Y/1 translocations are very rare, and have been reported in seven patients sofar. Pericentric inversions may be seen In all chromosomes and are not associated with phenotypic abnormalities. Here we report a 6-day old male baby with prenatal growth retardation, frontal bossing, hypertelorism. micrognathia, cleft soft palate, absent uvula, hypospadias, simian line in both hands and hammer toes. Cytogenetic analysis was performed with GTG-banding, C-banding and FISH analysis containing X centromeric probe, Yq12-qter locus specific probe and whole chromosome Y probe. An unbalanced Y/1 translocation was diagnosed: 45,X,der(1)inv(1)(p13:qter)t(y;1)(pter -> q11:p13),-Y.en_US
dc.language.isoenen_US
dc.publisherMedecine et Hygieneen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBiotechnology & applied microbiologyen_US
dc.subjectGenetics & heredityen_US
dc.subjectMedical ethicsen_US
dc.subjectResearch & experimental medicineen_US
dc.subjectUnbalanced Y/1 translocationen_US
dc.subjectY/autosome translocationen_US
dc.subjectPericentric inv(1)en_US
dc.subjectFamilial pericentric-inversionen_US
dc.subjectY-autosome translocationen_US
dc.subjectReciprocal translocationen_US
dc.subjectChromosome-1en_US
dc.subjectInfertilityen_US
dc.subjectSimiaeen_US
dc.subject.meshAbnormalities, multipleen_US
dc.subject.meshChromosome bandingen_US
dc.subject.meshChromosome deletionen_US
dc.subject.meshChromosomes, human, pair 1en_US
dc.subject.meshChromosomes, human, yen_US
dc.subject.meshCraniofacial abnormalitiesen_US
dc.subject.meshDNA mutational analysisen_US
dc.subject.meshHumansen_US
dc.subject.meshIn situ hybridization, fluorescenceen_US
dc.subject.meshInfant, newbornen_US
dc.subject.meshInversion, chromosomeen_US
dc.subject.meshKaryotypingen_US
dc.subject.meshMaleen_US
dc.subject.meshSeminal plasma proteinsen_US
dc.subject.meshSex chromosome aberrationsen_US
dc.subject.meshTranslocation, geneticen_US
dc.titleA dysmorphic newborn with 45,X,der(1)inv(1)(p13;qter)t(Y;1)(pter -> 4q11;p13),-Y De novo karyotypeen_US
dc.typeArticleen_US
dc.identifier.wos000230547700009tr_TR
dc.identifier.scopus2-s2.0-22444438011tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı.tr_TR
dc.identifier.startpage173tr_TR
dc.identifier.endpage177tr_TR
dc.identifier.volume16tr_TR
dc.identifier.issue2tr_TR
dc.relation.journalGenetic Counselingen_US
dc.contributor.buuauthorYakut, Tahsin-
dc.relation.collaborationYurt içitr_TR
dc.identifier.pubmed16080298tr_TR
dc.subject.wosBiotechnology & applied microbiologyen_US
dc.subject.wosMedicine, research & experimentalen_US
dc.subject.wosGenetics & heredityen_US
dc.subject.wosMedical ethicsen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubmeden_US
dc.wos.quartileQ4en_US
dc.contributor.scopusid6602802424tr_TR
dc.subject.scopusMale Sterility Due to Y-Chromosome Deletion; Azoospermia; Y Chromosomeen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeAutosomeen_US
dc.subject.emtreeC bandingen_US
dc.subject.emtreeCase reporten_US
dc.subject.emtreeCentromereen_US
dc.subject.emtreeChromosome 1en_US
dc.subject.emtreeChromosome analysisen_US
dc.subject.emtreeChromosome rearrangementen_US
dc.subject.emtreeChromosome translocationen_US
dc.subject.emtreeCleft palateen_US
dc.subject.emtreeCongenital malformationen_US
dc.subject.emtreeFrontal bossingen_US
dc.subject.emtreeGene locusen_US
dc.subject.emtreeGene probeen_US
dc.subject.emtreeGrowth retardationen_US
dc.subject.emtreeHammer toeen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeHypertelorismen_US
dc.subject.emtreeHypospadiasen_US
dc.subject.emtreeKaryotypeen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeMale infertilityen_US
dc.subject.emtreeMicrognathiaen_US
dc.subject.emtreeNewbornen_US
dc.subject.emtreePalatopharyngeal incompetenceen_US
dc.subject.emtreePericentric chromosome inversionen_US
dc.subject.emtreePhenotypeen_US
dc.subject.emtreePhysical examinationen_US
dc.subject.emtreeY chromosomeen_US
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