Prenatally Detected Maternally Inherited Partial Duplication of 11p15.5 ICR1 Results in Phenotypes Overlapping Russell‐Silver Syndrome in Infancy
Year: 2025
Type: article
Study design: Case Report
Source: Prenatal Diagnosis
DOI: 10.1002/pd.6832
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
Funder: Tow Foundation
OpenAlex ID: W4411295990
