Array-CGH analysis in patients with intellectual disability and/or congenital malformations in Brazil
Author:
Publisher
Genetics and Molecular Research
Subject
Genetics,Molecular Biology,General Medicine
Link
http://www.funpecrp.com.br/gmr/year2016/vol15-1/pdf/gmr7769.pdf
Cited by 11 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. Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in Brazil;Scientific Reports;2022-09-07
2. Genetic Analysis Algorithm for the Study of Patients with Multiple Congenital Anomalies and Isolated Congenital Heart Disease;Genes;2022-06-29
3. Chromosomal microarray analyses from 5,778 patients with neurodevelopmental disorders and congenital anomalies in Brazil;2022-03-10
4. Unravelling the genetic causes of multiple malformation syndromes: A whole exome sequencing study of the Cypriot population;PLOS ONE;2021-07-29
5. Implementation of chromosomal microarrays in a cohort of patients with intellectual disability at the Argentinean public health system;Molecular Biology Reports;2020-09
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