Citations for
1GTF2IL, GTF2IP1, GTF2IP2, PMS2L3, POM121L1, STAG3, STAG3L1, WBS
Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the williams-beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion.
Valero MC, de Luis O, Cruces J, Perez Jurado LA.
Genomics 69(1):1-13. 2000
2PMS2, PMS2L7, PMS2L8, PMS2LP1, PMS2L10, PMS2LP2, PMS2L11, PMS2L2, PMS2L3, PMS2L4, PMS2L5, PMS2L6, PMS2L7, UPK3B
Genomic organization of the human PMS2 gene family.
Nicolaides NC, Carter KC, Shell BK, Papadopoulos N, Vogelstein B, Kinzler KW.
Genomics 30(2):195-206. 1995
3HNPCC3, HNPCC4, PMS1, PMS2, PMS2L7, PMS2L8, PMS2L3, PMS2LP1, PMS2LP2
Mutations of two PMS homologues in hereditary nonpolyposis colon cancer.
Nicolaides NC, et al.
Nature 371 : 75-80. 1994
4PMS2, PMS2L1, PMS2L2, PMS2L3, PMS2L4, PMS2L5
Cloning, characterization and chromosomal assignment of the human genes homologous to yeast PMS1, a member of mismatch repair genes.
Horii A, et al.
Biochem Biophys Res Commun 204 : 1257-1264. 1994