Disease: Wolf-Hirschhorn syndrome

Definition: A chromosomal deletion syndrome that is characterized by distinct craniofacial features, hypotonia and intellectual disability and has_material_basis_in a hemizygous deletion of chromosome 4p16.3.

Synonyms: 4p deletion syndrome, chromosome 4p16.3 deletion syndrome, PITT SYNDROME, Pitt-Rogers-Danks Syndrome

OMIM: MIM:194190

Reagents:

Morpholino	Experiments
letm1 MO1	Xla Wt + letm1 MO Xla Wt + letm1 MO
nelfa MO1	Xla Wt + nelfa MO Xla Wt + nelfa MO Xla Wt + nelfa MO Xla Wt + nelfa MO
nsd2 MO1	Xla Wt + nsd2 MO Xla Wt + nsd2 MO Xla Wt + nsd2 MO Xla Wt + nsd2 MO
tacc3 MO2	Xla Wt + tacc3 MO Xla Wt + tacc3 MO Xla Wt + tacc3 MO Xla Wt + tacc3 MO Xla Wt + tacc3 MO