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A patient with a de-novo deletion 3p25.3 and features overlapping with Rubinstein-Taybi syndrome

dc.contributor.authorWagner, Nicholas
dc.contributor.authorKayserili, Hülya
dc.contributor.authorKuechler, Alma
dc.contributor.authorWieczorek, Dagmar
dc.contributor.authorLuedecke, Hermann-Josef
dc.contributor.authorCzeschik, Johanna Christina
dc.contributor.authorAlbrecht, Beate
dc.date.accessioned2021-03-05T11:38:57Z
dc.date.available2021-03-05T11:38:57Z
dc.date.issued2014
dc.identifier.citationCzeschik J. C. , Albrecht B., Kayserili H., Kuechler A., Wagner N., Wieczorek D., Luedecke H., "A patient with a de-novo deletion 3p25.3 and features overlapping with Rubinstein-Taybi syndrome", CLINICAL DYSMORPHOLOGY, cilt.23, ss.67-70, 2014
dc.identifier.issn0962-8827
dc.identifier.othervv_1032021
dc.identifier.otherav_a93645ab-04da-4c86-a9fb-fa3cf4949f8e
dc.identifier.urihttp://hdl.handle.net/20.500.12627/113037
dc.identifier.urihttps://doi.org/10.1097/mcd.0000000000000035
dc.language.isoeng
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.titleA patient with a de-novo deletion 3p25.3 and features overlapping with Rubinstein-Taybi syndrome
dc.typeMakale
dc.relation.journalCLINICAL DYSMORPHOLOGY
dc.contributor.departmentUniversity of Duisburg Essen , ,
dc.identifier.volume23
dc.identifier.issue2
dc.identifier.startpage67
dc.identifier.endpage70
dc.contributor.firstauthorID31694


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