1 | GTF2IL, GTF2IP1, GTF2IP2, PMS2L3, POM121L1, STAG3, STAG3L1, WBS
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| 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.
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| Valero MC, de Luis O, Cruces J, Perez Jurado LA.
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| Genomics 69(1):1-13. 2000
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2 | PMS2, PMS2L7, PMS2L8, PMS2LP1, PMS2L10, PMS2LP2, PMS2L11, PMS2L2, PMS2L3, PMS2L4, PMS2L5, PMS2L6, PMS2L7, UPK3B
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| Genomic organization of the human PMS2 gene family.
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| Nicolaides NC, Carter KC, Shell BK, Papadopoulos N, Vogelstein B, Kinzler KW.
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| Genomics 30(2):195-206. 1995
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3 | HNPCC3, HNPCC4, PMS1, PMS2, PMS2L7, PMS2L8, PMS2L3, PMS2LP1, PMS2LP2
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| Mutations of two PMS homologues in hereditary nonpolyposis colon cancer.
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| Nicolaides NC, et al.
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| Nature 371 : 75-80. 1994
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4 | PMS2, PMS2L1, PMS2L2, PMS2L3, PMS2L4, PMS2L5
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| Cloning, characterization and chromosomal assignment of the human genes homologous to yeast PMS1, a member of mismatch repair genes.
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| Horii A, et al.
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| Biochem Biophys Res Commun 204 : 1257-1264. 1994
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