WHCR FISH Probe

Wolf-Hirschhorn syndrome is a congenital malformation syndrome characterized by pre- and postnatal growth deficiency, developmental disability of variable degree, characteristic craniofacial features ('Greek warrior helmet' appearance of the nose, high forehead, prominent glabella, hypertelorism, high-arched eyebrows, protruding eyes, epicanthal folds, short philtrum, distinct mouth with downturned corners, and micrognathia), and a seizure disorder (Battaglia et al., 2008 [PubMed 18932224]).[supplied by OMIM, Nov 2010]


Gene Details
SKU Test Kits Buffer Dye Color Order Now
WHCR-20-RE 20 (40 μL) 200 μL color Request Pricing
WHCR-20-OR 20 (40 μL) 200 μL color Request Pricing
WHCR-20-GO 20 (40 μL) 200 μL color Request Pricing
WHCR-20-GR 20 (40 μL) 200 μL color Request Pricing
WHCR-20-AQ 20 (40 μL) 200 μL color Request Pricing

Gene Summary

Wolf-Hirschhorn syndrome is a congenital malformation syndrome characterized by pre- and postnatal growth deficiency, developmental disability of variable degree, characteristic craniofacial features ('Greek warrior helmet' appearance of the nose, high forehead, prominent glabella, hypertelorism, high-arched eyebrows, protruding eyes, epicanthal folds, short philtrum, distinct mouth with downturned corners, and micrognathia), and a seizure disorder (Battaglia et al., 2008 [PubMed 18932224]).[supplied by OMIM, Nov 2010]

Gene Details

Gene Symbol : WHCR

Gene Name : Wolf-Hirschhorn syndrome chromosome region

Chromosome : CHR 4: 0-0

Locus : 4p16

Request Pricing

Lorem Ipsum is simply dummy text of the printing and typesetting industry.

Lorem Ipsum is simply dummy text of the printing and typesetting industry.