PMC:1440874 / 60159-60642 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PMC/sourceid/1440874","sourcedb":"PMC","sourceid":"1440874","source_url":"http://www.ncbi.nlm.nih.gov/pmc/1440874","text":"The Online Mendelian Inheritance in Man (http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=OMIM) accession number for ATR-X syndrome is 301040. The GeneID (www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=gene) for human ATRX is 546 and for mouse Atrx is 22589. The GenBank (http://www.ncbi.nlm.nih.gov/) accession number for the minor satellite probe mCENT2 is X14470 (nucleotides 75–101), for the major satellite probe DG27 is M25032 (nucleotides 146–172), and for the IAP probe is L33247.","tracks":[]}