Noonan syndrome due to a SHOC2 mutation presenting with fetal distress and fatal hypertrophic cardiomyopathy in a premature infant
Year: 2012
Type: article
Study design: Case Report
DOI: 10.1002/ajmg.a.35318
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2126217107
