ID   HH0134
AC   CVCL_8X27
DR   ECACC; 89061429
DR   Wikidata; Q54887420
CC   Part of: ECACC chromosomal abnormality collection.
CC   Population: Caucasian.
CC   Derived from site: In situ; Amniotic fluid; UBERON=UBERON_0000173.
DI   NCIt; C84717; Fragile X syndrome
DI   ORDO; Orphanet_908; Fragile X syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Sex unspecified
AG   Fetus
CA   Finite cell line
DT   Created: 23-02-16; Last updated: 29-06-23; Version: 8
//