Literature DB >> 21108406

Delineation of the breakpoints of pure duplication 3q due to a de novo duplication event using SOMA.

A L Shanske1, J Leonard, O Nahum, D L Coppock, B Levy.   

Abstract

Mesh：

Year:  2010        PMID： 21108406     DOI： 10.1002/ajmg.a.33431

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


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  3 in total

1.  A Pure 2-Mb 3q26.2 Duplication Proximal to the Critical Region of 3q Duplication Syndrome.

Authors:  Miriam Coelho Molck; Milena Simioni; Társis Paiva Vieira; Fabíola Paoli Monteiro; Vera L Gil-da-Silva-Lopes
Journal:  Mol Syndromol       Date:  2018-06-08

2.  Clinical, Cytogenetic, and Biochemical Analyses of a Family with a t(3;13)(q26.2;p11.2): Further Delineation of 3q Duplication Syndrome.

Authors:  M Abreu-González; C García-Delgado; A Cervantes; A Aparicio-Onofre; R Guevara-Yáñez; R Sánchez-Urbina; M P Gallegos-Arreola; A Luna-Angulo; F J Estrada; V F Morán-Barroso
Journal:  Case Rep Genet       Date:  2013-09-18

3.  Rare de novo inversion-duplication case with pure 3qter duplication syndrome including an overlap of the dup(3q) critical region: A case report.

Authors:  George Imataka; Yoshiyuki Watabe; Sayuri Kajitani; Shun Watanabe; Junko Ichikawa; Fabrizio Drago; Hiroshi Suzumura; Shigemi Yoshihara
Journal:  Exp Ther Med       Date:  2017-05-03       Impact factor: 2.447
  3 in total

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