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Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22.
Hum Mol Genet. 1994 Aug;3(8):1217-25. doi: 10.1093/hmg/3.8.1217.
Hum Mol Genet. 1994.
PMID: 7987295
A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10.
Angrist M, Kauffman E, Slaugenhaupt SA, Matise TC, Puffenberger EG, Washington SS, Lipson A, Cass DT, Reyna T, Weeks DE, et al.
Angrist M, et al.
Nat Genet. 1993 Aug;4(4):351-6. doi: 10.1038/ng0893-351.
Nat Genet. 1993.
PMID: 8401581
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Y chromosome sequence variation and the history of human populations.
Underhill PA, Shen P, Lin AA, Jin L, Passarino G, Yang WH, Kauffman E, Bonné-Tamir B, Bertranpetit J, Francalacci P, Ibrahim M, Jenkins T, Kidd JR, Mehdi SQ, Seielstad MT, Wells RS, Piazza A, Davis RW, Feldman MW, Cavalli-Sforza LL, Oefner PJ.
Underhill PA, et al.
Nat Genet. 2000 Nov;26(3):358-61. doi: 10.1038/81685.
Nat Genet. 2000.
PMID: 11062480
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