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Deletion 18p Syndrome
A rare genetic syndrome characterized by the deletion of the short arm of chromosome 18. It is associated with mental and growth retardation, prominent ears and ptosis. (NCI Thesaurus)
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Elimination, especially by blotting out, cutting out, or erasing.
A mutation that is documented to be associated with risk of disease.
Deleted in Malignant Brain Tumors 1, encoded by the human DMBT1 gene, is a member of the scavenger-receptor superfamily and likely a…
Deleted in bladder cancer protein 1 (761 aa, ~89 kDa) is encoded by the human DBC1 gene. This protein is involved in…
To entrust to another.
A person appointed or elected to represent others.
