Case of interstitial 12q deletion in association with Wilms tumor
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference24 articles.
1. Wilms' tumor, malformative syndrome, mental retardation and de novo constitutional translocation, t(7;13)(q36;q13)
2. Value of chromosome painting in determining the chromosomal outcome in offspring of a 12;16 translocation carrier.
3. Comprehensive Human Genetic Maps: Individual and Sex-Specific Variation in Recombination
4. Clinical phenotype associated with terminal 2q37 deletion
Cited by 12 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. Comparative Genomic Mapping Implicates LRRK2 for Intellectual Disability and Autism at 12q12, and HDHD1, as Well as PNPLA4, for X-Linked Intellectual Disability at Xp22.31;Journal of Clinical Medicine;2020-01-19
2. Haploinsufficiency ofANO6, NELL2andDBX2in a boy with intellectual disability and growth delay;American Journal of Medical Genetics Part A;2015-04-06
3. 12q21.2q22 deletion: A new patient;American Journal of Medical Genetics Part A;2015-04-06
4. Genetic Predisposition to Wilms Tumour;Renal Tumors of Childhood;2014
5. A family with a 1.17 Mb deletion of 12q12: Refining genotype-phenotype correlation;American Journal of Medical Genetics Part A;2010-08-03
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