?Tandem? duplication of 4p16.1p16.3 chromosome region associated with 4p16.3pter molecular deletion resulting in Wolf-Hirschhorn syndrome phenotype
Year: 1999
Type: article
Study design: Case Report
Authors: M. Zollino, T.J. Wright, C. Di Stefano, A. Tosolini, A. Battaglia, M.R. Altherr, G. Neri
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2044330393
