Literature DB >> 1022850

[Partial "de novo" trisomy 10q (author's transl)].

R Berger, J Derre, M Murawsky, C Amiel-Tison.   

Abstract

A partial 10q trisomy due to a de novo t(10;22) translocation is reported. The comparison with other published cases of partial 10q trisomy leads to the description of a particular syndrome essentially due to a trisomy for bands 10q24 to 10q26.

Entities:  

Mesh：

Year:  1976        PMID： 1022850

Source DB:  PubMed          Journal:  J Genet Hum        ISSN： 0021-7743


  5 in total

1.  Severe mental retardation in six generations of a large South African family carrying a translocation t(6;10)(q27;q25.2).

Authors:  J Brusnický; K M van Heerden; G de Jong; A S Cronjé; A E Retief
Journal:  J Med Genet       Date:  1986-10       Impact factor: 6.318

2.  Partial trisomy 10q: a recognizable syndrome.

Authors:  J M Klep-de Pater; J B Bijlsma; H F de France; N J Leschot; M Duijndam-van den Berge; J O van Hemel
Journal:  Hum Genet       Date:  1979-01-19       Impact factor: 4.132

3.  Partial trisomy 11q as the result of sporadic translocation.

Authors:  I W Lurie; G I Lazjuk; Y I Usova; D B Gurevich
Journal:  Hum Genet       Date:  1979-09-02       Impact factor: 4.132

4.  Confirmation of a de novo duplication, dup(10)(q24 leads to q26), by GOT1 gene dosage studies.

Authors:  D J Tomkins; B J Gitelman; M H Roberts
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

5.  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
  5 in total

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