Three probands with autistic disorder and isodicentric chromosome 15

Author(s):  
Chantelle M. Wolpert ◽  
Marisa M. Menold ◽  
Meredyth P. Bass ◽  
Mazin B. Qumsiyeh ◽  
Shannon L. Donnelly ◽  
...  
2012 ◽  
Vol 55 (12) ◽  
pp. 487 ◽  
Author(s):  
Jon Soo Kim ◽  
Jinyu Park ◽  
Byung-Joo Min ◽  
Sun Kyung Oh ◽  
Jin Sun Choi ◽  
...  

2014 ◽  
Vol 40 (6) ◽  
pp. 1795-1798 ◽  
Author(s):  
Taro Nonaka ◽  
Izumi Ooki ◽  
Takayuki Enomoto ◽  
Koichi Takakuwa

2001 ◽  
Vol 15 (3-4) ◽  
pp. 245-259 ◽  
Author(s):  
Marisa M. Menold ◽  
Yujun Shao ◽  
Chantelle M. Wolpert ◽  
Shannon L. Donnelly ◽  
Kimberly L. Raiford ◽  
...  

2007 ◽  
Vol 2007 ◽  
pp. 1-4 ◽  
Author(s):  
Karim Ouldim ◽  
Abdelhafid Natiq ◽  
Philippe Jonveaux ◽  
Abdelaziz Sefiani

We report the case of a Moroccan boy with mental retardation, hyperactivity, epilepsy, developmental problems and behavioural disorders. Cytogenetic analysis showed the presence of a supernumerary marker chromosome. Molecular cytogenetics allowed us to determine the marker as an inverted duplication of chromosome 15. It is the first case of a Moroccan patient with tetrasomy 15q in which fluorescence in situ hybridization (FISH) enabled us to specify the diagnosis. Interestingly, this patient has an infantile autism with cytogenetic abnormalities on chromosomal region 15q11-q13 as reported in patients with Autistic Disorder.


2015 ◽  
Vol 35 (4) ◽  
pp. 474-476
Author(s):  
John Hoon Rim ◽  
Hee Jung Chung ◽  
Saeam Shin ◽  
Seo-Jin Park ◽  
Jong Rak Choi

2019 ◽  
Vol 235-236 ◽  
pp. 93-94
Author(s):  
Roberto Antonucci ◽  
Nadia Vacca ◽  
Elisa Ghisu ◽  
Gloria Acquaviva ◽  
Carlo Cosmi ◽  
...  

Neurogenetics ◽  
2000 ◽  
Vol 2 (4) ◽  
pp. 219-226 ◽  
Author(s):  
M. P. Bass ◽  
M. M. Menold ◽  
C. M. Wolpert ◽  
S. L. Donnelly ◽  
S. A. Ravan ◽  
...  

Author(s):  
Chantelle Wolpert ◽  
Margaret A. Pericak-Vance ◽  
Ruth K. Abramson ◽  
Harry H. Wright ◽  
Michael L. Cuccaro

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