Chrome Extension
WeChat Mini Program
Use on ChatGLM
VIPCreated with Sketch.

Phenotypic Heterogeneity in 22q11.2 Deletion Syndrome: Copy Number Variants As Genetic Modifiers for Congenital Heart Disease in a Brazilian Cohort

M. Zamariolli,A. G. Dantas,N. Nunes,M. Moyses-Oliveira,I. C. Sgardioli,D. C. Q. Soares,V. L. Gil-Da-Silva-Lopes,C. A. Kim,M. I. Melaragno

American Journal of Medical Genetics Part A（2023）

Cited 0|Views20
Key words
22q11,2 deletion syndrome,congenital heart disease (CHD),copy-number variant (CNV),genetic modifiers
AI Read Science
Must-Reading Tree
Example
Generate MRT to find the research sequence of this paper
Chat Paper
Summary is being generated by the instructions you defined