Trisomy 12p syndrome secondary to a balanced familial translocation-Reference-Cited by-同舟云学术

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Trisomy 12p syndrome secondary to a balanced familial translocation

Published:2009-09-28 Issue:3 Volume:52 Page:e144-e146
ISSN:1328-8067
Container-title:Pediatrics International
language:en
Short-container-title:

Author:

Zen Paulo Ricardo Gazzola,Rosa Rafael Fabiano Machado,Rosa Rosana Cardoso Manique,Graziadio Carla,Paskulin Giorgio Adriano

Publisher

Wiley

Subject

Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1442-200X.2010.03061.x/fullpdf

Reference10 articles.

1. Genotype/phenotype analysis in a patient with pure and complete trisomy 12p;Zumkeller;Am. J. Med. Genet.,2004

2. The natural history of trisomy 12p;Segel;Am. J. Med. Genet.,2006

3. Identification of partial 12 trisomy by quinacrine fluorescence;Uchida;J. Pediatr.,1973

4. Two cases of trisomy 12p due to rcpt (12;21)(p11;p11) inherited through three generations;Parslow;Hum. Genet.,1979

5. New chromosomal dysmorphic syndromes.4. Trisomy 12 p;Stengel-Rutkowski;Eur. J. Pediatr.,1981

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Trisomy of the Short Arm of Chromosome 12 Associated with High Cardiovascular Risk: A Case Report;High Blood Pressure & Cardiovascular Prevention;2019-02-26

2. A new partial trisomy 12p with artery catheter vagus, congenital cataracts, external auditory canal, and no turbinate;Gene;2012-11

3. Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes;European Journal of Medical Genetics;2012-08

4. A new partial trisomy 12p with artery catheter vagus, congenital cataract, no turbinate and external auditory canal;Journal of Medical Colleges of PLA;2012-04

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