De Novo 21q22.1q22.2 deletion including RUNX1 mimicking a congenital infection
Year: 2010
Type: article
DOI: 10.1002/ajmg.a.33809
Institution: CHU Dijon Bourgogne
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W1985309106
