Literature DB >> 11310998

Molecular cytogenetics and phenotype characterization of a de novo pure partial trisomy 10(q24.33-qter).

E Petek, G Köstl, L Rauter, I Mutz, K Wagner, P M Kroisel.   

Abstract

The molecular-cytogenetic characterization of a de novo pure partial trisomy 10(q24.33-qter) is described. This report provides information about the postnatal phenotype. The clinical findings observed in this case support the conclusion that the more severe disease related genes are located between 10q24.1 and q24.33.

Mesh:

Year:  2001        PMID: 11310998     DOI: 10.1097/00019605-200104000-00015

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN: 0962-8827            Impact factor:   0.816


  2 in total

1.  Inverted Duplication and Deletion of 10q25q26 in a Patient without Any Obvious Skeletal Anomalies.

Authors:  B Xiao; X Ji; Y Xing; W-T Jiang; J-M Zhang; J Tao
Journal:  Mol Syndromol       Date:  2012-09-27

2.  Distal trisomy 10q syndrome, report of a patient with duplicated q24.31 - qter, autism spectrum disorder and unusual features.

Authors:  Yasser Al-Sarraj; Hakam Abu Al-Khair; Rowaida Ziad Taha; Namat Khattab; Zakaria H El Sayed; Bushra Elhusein; Hatem El-Shanti
Journal:  Clin Case Rep       Date:  2014-07-25
  2 in total

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