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Rare Cancer-Associated Syndrome
A broad classification for uncommon disorders in which the development of neoplasms occur in association with a characteristic set of signs or symptoms. These disorders commonly have a genetic basis. The types of neoplasms themselves are not necessarily uncommon. (NCI Thesaurus)
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Human RARB wild-type allele is located within 3p24 and is approximately 170 kb in length. This allele, which encodes retinoic acid receptor…
This gene is involved in the regulation of embryonic morphogenesis and related processes.
A fusion protein encoded by the RARA/ZBTB16 fusion gene. This protein is comprised of the N-terminal transcriptional activation domain of the retinoic…
A fusion gene that results from a chromosomal translocation t(11;17)(q23;q21) which fuses the exon 3 of the RARA gene to the 3'…
A fusion gene that results from a chromosomal translocation t(15;17)(q22;q21) which fuses the first 2 exons of the RARA gene with the…
Human RARA wild-type allele is located within 17q21 and is approximately 48 kb in length. This allele, which encodes retinoic acid receptor…
