Literature DB >> 7447607

[Retinoblastoma and interstitial deletion of 13q (author's transl)].

J De Grouchy, C Turleau, M O Cabanis, J M Richardet.   

Abstract

The authors report an observation of retinoblastoma associated with partial monosomy 13q [46, XY, t (2;10) (q21;q24), inv(9), del(13)(q13q213)] and discuss the origin of this exceptional childhood tumor by gene mutation of chromosome rearrangement.

Entities:  

Mesh：

Year:  1980        PMID： 7447607

Source DB:  PubMed          Journal:  Arch Fr Pediatr        ISSN： 0003-9764


  4 in total

Review 1.  13q13.1-q13.2 deletion in tetralogy of Fallot: clinical report and a literature review.

Authors:  Gregory Costain; Candice K Silversides; Christian R Marshall; Mary Shago; Nicholas Costain; Anne S Bassett
Journal:  Int J Cardiol       Date:  2010-07-03       Impact factor: 4.164

2.  The genetics of retinoblastoma, revisited.

Authors:  A Naumova; C Sapienza
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

3.  A recognizable pattern of the midface of retinoblastoma patients with interstitial deletion of 13q.

Authors:  T Motegi; M Kaga; Y Yanagawa; H Kadowaki; K Watanabe; A Inoue; M Komatsu; K Minoda
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

4.  Retinoblastoma-del(13q14): report of two patients, one with a trisomic sib due to maternal insertion. Gene-dosage effect for esterase D.

Authors:  H Rivera; C Turleau; J de Grouchy; C Junien; S Despoisse; J M Zucker
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.