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Nzoz genomed > Genetic tests > Tests list

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Genetic testing

Microdeletion Syndromes

Genetic Testing Offered by NZOZ Genomed

Test DescriptionThe CodePriceTurnaround time
Microdeletion Syndromes
Microdeletion 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 into a morphological tube containing EDTA
MICDEL-1 700.00 zł up to 5 weeks
Microdeletion Syndromes
Microdeletion syndromes analysis: 1q21.1 (TAR syndrome), 1q21.1 (regions other than TAR), 3q29, 7q36.1 (CNTNAP2 gene), 12p11.23 (involved in schizophrenia), 15q13, 15q24.1 (PML gene, outside 15q24 syndrome), 16p11, 17q12, 18q21.2 (TCF4 gene), 20p12.2 (PAK7 gene) by MLPA 1
   We perform genetic testing from:
  • venous blood collected into a morphological tube containing EDTA
MICDEL-2 700.00 zł up to 5 weeks



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