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Phenotypic variability in a Hungarian patient with the 4q21 microdeletion syndrome
Komlósi, Katalin, Duga, Balázs, Hadzsiev, Kinga, Czakó, Márta, Kosztolányi, György, Fogarasi, András, Melegh, BélaVolume:
8
Year:
2015
Language:
english
Journal:
Molecular Cytogenetics
DOI:
10.1186/s13039-015-0118-7
File:
PDF, 923 KB
english, 2015