Microdeletion Probes
Description: The SHOX region probe is optimized to detect copy numbers of the SHOX gene region at Xp22. The ...
Description: Smith-Magenis syndrome (SMS) is a multiple congenital anomaly syndrome characterised by mental ...
Description: SMS is approximately 140 kb in size and homologous to the Smith-Magenis region. The SMS probe is ...
Description: Smith-Magenis syndrome (SMS) is a multiple congenital anomaly syndrome characterised by mental ...
Description: NSD1 (5q35) SpectrumOrange Probe Set hybridized to a metaphase cell.
Description: The SRY gene is located within 10kb of the psuedoautosomal region of Yp. The LSI SRY probe is ...
Description: SRY (sex-determining region Y) located in band Yp11.31 is the genetic master switch of gonadal ...
Description: STS may be used to identify deletions of the STS gene located in band Xp22.3. This mixture contains ...
Description: Targeting 7q11.23, the Elastin gene (ELN) gene region, the Williams (ELN) Region Probe consists of ...
Description: The ELN region probe is optimized to detect copy numbers of the ELN gene region at 7q11. The 7q22 ...
Description: Williams-Beuren Syndrome (WBS) is a developmental disorder caused by a microdeletion of 7q11.23. ...
Description: Wolf-Hirschhorn syndrome is a multiple malformation syndrome characterised by severe growth ...
Description: The Wolf-Hirschhorn (WHS) probe set targets p arm of chromosome 4. The WHS probe is directly ...
Description: The WHSC1 region probe is optimized to detect copy numbers of the critical region at 4p16. The ...
Description: The XIST specific DNA probe is optimized to detect copy numbers of the XIST region at Xq13. The ...
Description: One X chromosome is inactivated (Xi) in each cell of a female in order to achieve transcriptional ...