A leading provider of
innovative DNA Screening solutions
Wolf-Hirschhorn LPU009
Wolf-Hirschhorn syndrome is caused by a partial deletion of chromosome 4. It is characterised by severe growth deficiency, severe to profound mental retardation with the onset of convulsions in early infancy, microcephaly, sacral dimples and characteristic facies ('Greek helmet appearance'). The Cytocell probe has been designed to target both Wolf-Hirschhorn critical regions.
Wolf-Hirschhorn (WHSCR) Probe
Cat. No. LPU 009-S (5 tests)
Cat. No. LPU 009 (10 tests)
This webpage could contain information on product details or information not valid in your country or region. Please be aware that we do not take any responsibility for accessing such information, which may not comply with any legal process, regulation, registration or usage in the country of your origin. If you are a resident of a country other than those to which this site is directed, contact your local Cytocell distributor to obtain the appropriate product information for your country of residence.
Developed &produced in the UK