Molecular characterization of near-complete trisomy 17p syndrome from inverted duplication in association with cryptic deletion of 17pter
Year: 2014
Type: article
Study design: Case Report
Source: Gene
Institutions: Samsung Medical Center, Sungkyunkwan University
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W1995230798
