![](/img/cover-not-exists.png)
Unique Combination of 22q11 and 14qter Microdeletion Syndromes Detected Using Oligonucleotide Array-CGH
Zrnová, E., Vranová, V., Šoukalová, J., Slámová, I., Vilémová, M., Gaillyová, R., Kuglík, P.Volume:
2
Year:
2011
Language:
english
Journal:
Molecular Syndromology
DOI:
10.1159/000335334
File:
PDF, 1.51 MB
english, 2011