The incidence of a deletion in chromosome 22Q11 in sporadic and familial conotruncal heart disease
Year: 1996
Type: article
Source: European Journal of Pediatrics
DOI: 10.1007/bf01957162
Authors: K. Devriendt, B. Eyskens, A. Swillen, M. Dumoulin, M. Gewillig, J. -P. Fryns
Institutions: Universitair Ziekenhuis Leuven, KU Leuven
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2014038820