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Aarskog syndrome: expanding the phenotypic and molecular spectrum through a new case series including two adult patients

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dc.conference.dateJUN 01-04, 2024
dc.conference.locationBerlin, GERMANY
dc.contributor.coauthorTurgut, Gozde Tutku
dc.contributor.coauthorKalayci, Tugba
dc.contributor.coauthorAslanger, Ayca Dilruba
dc.contributor.coauthorKaraman, Volkan
dc.contributor.coauthorUyguner, Zehra Oya
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorAltunoğlu, Umut
dc.contributor.kuauthorAvcı, Şahin
dc.contributor.kuauthorKayserili, Hülya
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2026-01-09T06:07:05Z
dc.date.available2026-01-09
dc.date.issued2024
dc.description.fulltextNo
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.identifier.eissn1476-5438
dc.identifier.embargoNo
dc.identifier.endpage1133
dc.identifier.issn1018-4813
dc.identifier.quartileQ1
dc.identifier.scopusN/A
dc.identifier.startpage1133
dc.identifier.urihttps://hdl.handle.net/20.500.14288/31905
dc.identifier.volume32
dc.identifier.wos001421430501021
dc.language.isoeng
dc.publisherSpringerNature
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofEuropean Journal of Human Genetics
dc.relation.ispartof57th Conference of the European-Society-of-Human-Genetics (ESHG)
dc.relation.openaccessNo
dc.rightsCopyrighted
dc.subjectBiochemistry and molecular biology
dc.subjectGenetics and heredity
dc.titleAarskog syndrome: expanding the phenotypic and molecular spectrum through a new case series including two adult patients
dc.typeMeeting Abstract
dspace.entity.typePublication
person.familyNameAltunoğlu
person.familyNameAvcı
person.familyNameKayserili
person.givenNameUmut
person.givenNameŞahin
person.givenNameHülya
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relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

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