| 1 | PMS2, PMS2L8, PMS2L11, PMS2LP1, PMS2LP2, WBS
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| PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7.
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| Osborne LR, Herbrick JA, Greavette T, Heng HH, Tsui LC, Scherer SW.
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| Genomics 45(2):402-6. 1997
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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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