scholarly journals The restriction endonuclease Tru9I is a useful tool to analyze telomere sequences separately from interstitial telomeric sequences in <i>Arabidopsis thaliana</i>

2012 ◽  
Vol 02 (03) ◽  
pp. 242-244 ◽  
Author(s):  
María I. Vaquero-Sedas ◽  
Miguel A. Vega-Palas
2014 ◽  
Vol 167 (2) ◽  
pp. 428-433 ◽  
Author(s):  
Jonathan Lévy ◽  
Aline Receveur ◽  
Guillaume Jedraszak ◽  
Sandra Chantot-Bastaraud ◽  
Florence Renaldo ◽  
...  

2012 ◽  
Vol 55 (12) ◽  
pp. 1029-1037 ◽  
Author(s):  
GuangZhen Ji ◽  
Kai Liu ◽  
ChengBin Chen ◽  
WeiMin Ruan ◽  
Christina Glytsou ◽  
...  

Author(s):  
Gavin Cuthbert ◽  
Simon McCullough ◽  
Roger Finney ◽  
Gareth Breese ◽  
Nick Bown

2013 ◽  
Vol 110 (49) ◽  
pp. 19866-19871 ◽  
Author(s):  
A. Y. Aksenova ◽  
P. W. Greenwell ◽  
M. Dominska ◽  
A. A. Shishkin ◽  
J. C. Kim ◽  
...  

1993 ◽  
Vol 30 (11) ◽  
pp. 926-931 ◽  
Author(s):  
E Rossi ◽  
G Floridia ◽  
M Casali ◽  
C Danesino ◽  
G Chiumello ◽  
...  

2017 ◽  
Vol 153 (3) ◽  
pp. 117-124 ◽  
Author(s):  
Lyvia Marlet ◽  
Eudeline Alix ◽  
Marianne Till ◽  
Fabienne Raskin-Champion ◽  
Jocelyne Attia ◽  
...  

We report on a prenatally diagnosed unusual case of inverted terminal duplication of the short arm of chromosome 2, leading to interstitial telomeric sequences (ITSs) and partial trisomy 2p. To our knowledge, there are only 4 further cases of pure partial trisomy 2p reported prenatally. Here, the mother was referred at 22 weeks of gestation for isolated fetal congenital heart malformation at ultrasound. The karyotype of amniotic fluid cells displayed a large duplication of the short arm of chromosome 2 that was further investigated by array-CGH, which detected a 1-copy gain of 43.75 Mb in chromosome 2 at 2p21p25.3. FISH confirmed the presence of an inverted duplication in the short arm of chromosome 2 involving the region 2p21pter and revealed the presence of ITSs at the breakpoint in chromosome 2p21. This report contributes to the prenatal description of the syndrome. We also discuss the possible mechanisms leading to this duplication and the formation of ITSs which are rarely described in constitutional rearrangements.


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