학술논문
A familial chromosomal complex rearrangement confirms RUNX1T1 as a causative gene for intellectual disability and suggests that 1p22.1p21.3 duplication is likely benign
Document Type
Article
Author
Source
In: Molecular Cytogenetics . (Molecular Cytogenetics, 14 June 2019, 12(1))
Subject
Language
English
ISSN
17558166