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A case with Prader-Willi phenotype and a de novo t(2;15)(q31;p11)

dc.contributor.authorAcar, Hasan
dc.contributor.authorKALAYCI YİĞİN, Aysel
dc.contributor.authorAtabek, Emre
dc.contributor.authorCORA, Tülin
dc.date.accessioned2021-03-03T14:40:05Z
dc.date.available2021-03-03T14:40:05Z
dc.identifier.citationCORA T., Acar H., KALAYCI YİĞİN A., Atabek E., "A case with Prader-Willi phenotype and a de novo t(2;15)(q31;p11)", 39th European Human Genetics Conference, Nice, Fransa, 16 - 19 Haziran 2007, ss.1
dc.identifier.othervv_1032021
dc.identifier.otherav_3ac38421-f526-4d9c-85b7-02db2524f952
dc.identifier.urihttp://hdl.handle.net/20.500.12627/43486
dc.language.isoeng
dc.subjectTemel Bilimler
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.titleA case with Prader-Willi phenotype and a de novo t(2;15)(q31;p11)
dc.typeBildiri
dc.contributor.departmentSelçuk Üniversitesi , ,
dc.contributor.firstauthorID392304


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