WeChat Mini Program
Old Version Features

Clinical Evaluation of Rare Copy Number Variations Identified by Chromosomal Microarray in a Hungarian Neurodevelopmental Disorder Patient Cohort.

Anna Lengyel,Éva Pinti,Henriett Pikó,Árvai Kristóf,Tünde Abonyi,Zaránd Némethi,György Fekete,Irén Haltrich

Molecular Cytogenetics（2022）

Cited 2|Views21
Key words
Neurodevelopmental disorders,Chromosomal microarray,14q11.2 microdeletion,Variants of unknown significance,PPP3CA,SYNDIG1
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