Interstitial 8p deletion in two patients with the expansion of phenotype and possibility of contribution of PINX1 gene and GATA4 rs3729856 variant in absent nails
Year: 2024
Type: article
Study design: Case Report
Institutions: National Research Centre, National Research Council Canada
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W4404775165
