Chrome Extension
WeChat Mini Program
Use on ChatGLM

Inherited Cases of CNOT3‐associated Intellectual Developmental Disorder with Speech Delay, Autism, and Dysmorphic Facies

Clinical Genetics(2020)

Cited 12|Views34
Key words
CNOT3,familial transmission,intellectual disability,neurodevelopmental disorder,whole-exome sequencing
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