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Year | Number of Results |
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2002 | 1 |
2007 | 1 |
2008 | 2 |
2024 | 0 |
PubMed (cited) for id: 606874
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Mapping of a Hirschsprung's disease locus in 3p21.
Eur J Hum Genet. 2008 Jul;16(7):833-40. doi: 10.1038/ejhg.2008.18. Epub 2008 Feb 20.
Eur J Hum Genet. 2008.
PMID: 18285831
Hirschsprung disease, associated syndromes and genetics: a review.
Amiel J, Sproat-Emison E, Garcia-Barcelo M, Lantieri F, Burzynski G, Borrego S, Pelet A, Arnold S, Miao X, Griseri P, Brooks AS, Antinolo G, de Pontual L, Clement-Ziza M, Munnich A, Kashuk C, West K, Wong KK, Lyonnet S, Chakravarti A, Tam PK, Ceccherini I, Hofstra RM, Fernandez R; Hirschsprung Disease Consortium.
Amiel J, et al.
J Med Genet. 2008 Jan;45(1):1-14. doi: 10.1136/jmg.2007.053959. Epub 2007 Oct 26.
J Med Genet. 2008.
PMID: 17965226
Review.
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Segregation at three loci explains familial and population risk in Hirschsprung disease.
Gabriel SB, Salomon R, Pelet A, Angrist M, Amiel J, Fornage M, Attié-Bitach T, Olson JM, Hofstra R, Buys C, Steffann J, Munnich A, Lyonnet S, Chakravarti A.
Gabriel SB, et al.
Nat Genet. 2002 May;31(1):89-93. doi: 10.1038/ng868. Epub 2002 Apr 15.
Nat Genet. 2002.
PMID: 11953745
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