A case of de novo trisomy 12p syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1989.tb02958.x/fullpdf
Reference8 articles.
1. Double translocation t(7;12), t(2;6) heterozygosity in one family;Bijlsma;Hum. Genet.,1978
2. De novo occurrence of mosaic trisomy 12p in a mentally retarded boy;Kondo;Hum. Genet.,1979
3. Two cases of trisomy 12p due to rect(12;21)(p11;p11) inherited through three generations;Parslow;Hum. Genet.,1979
4. A case of de novo trisomy 12p syndrome;Ray;Ann. Genet. (Paris),1985
5. Centric fusion, centromere-telomere fusion and isochromosome formation: a possible origin of a de novo 12p trisomy;Rivera;Clin. Genet.,1987
Cited by 14 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. Report on 3 patients with 12p duplication including GRIN2B;European Journal of Medical Genetics;2014-04
2. De novo trisomy 12p in twin girls with different levels of mosaicism;American Journal of Medical Genetics Part A;2013-05-17
3. Duplication 12p and Pallister-Killian syndrome: A case report and review of the literature toward defining a Pallister-Killian syndrome minimal critical region;American Journal of Medical Genetics Part A;2012-11-20
4. A new partial trisomy 12p with artery catheter vagus, congenital cataracts, external auditory canal, and no turbinate;Gene;2012-11
5. Pure and complete 12p trisomy due to a maternal centric fission of chromosome 12;American Journal of Medical Genetics Part A;2011-01-13
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