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NZOZ genomed
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Genetic testing
> Microdeletion Syndromes
Genetic testing
Genetic testing
Waluta
Microdeletion Syndromes
Microdeletion Syndromes
Test code: MICDEL-1Microdeletion syndromes analysis: 1p36, 2p16, 2q23/MBD5, 2q33/SATB2, 3q29, 9q22.3, 15q24, 17q21, 22q13/Phelan-McDermid, 5p15 (Cri du Chat syndrome), 22q11 (DiGeorge syndrome), 22q11 dystal region, 10p15, 8q (Langer-Giedion syndrome), 17p (Miller-Dieker syndrome), NF1, Prader-Willi/ Angelman syndrome, MECP2 duplication / Xq28, Rubinstein-Taybi syndrome, Smith-Magenis syndrome, 5q35.3 (Sotos syndrome), Williams syndrome, 4p16.3 (Wolf-Hirschhorn syndrome) by MLPA 1
We perform genetic testing from:
venous blood collected
Microdeletion Syndromes
Diagnostyka wybranych zespołów mikrodelecyjnych/mikroduplikacji metodą MLPA



