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Volumn 84, Issue 1, 2013, Pages 94-96

BMPR1A mutations in early-onset colorectal cancer with mismatch repair proficiency

Author keywords

[No Author keywords available]

Indexed keywords

BONE MORPHOGENETIC PROTEIN RECEPTOR 1A;

EID: 84879842001     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/cge.12023     Document Type: Letter
Times cited : (11)

References (6)
  • 1
    • 79959982314 scopus 로고    scopus 로고
    • BMPR1A mutations in hereditary nonpolyposis colorectal cancer without mismatch repair deficiency
    • Nieminen TT, Abdel-Rahman WM, Ristimaki A et al. BMPR1A mutations in hereditary nonpolyposis colorectal cancer without mismatch repair deficiency. Gastroenterology 2011: 141: e23-e26.
    • (2011) Gastroenterology , vol.141
    • Nieminen, T.T.1    Abdel-Rahman, W.M.2    Ristimaki, A.3
  • 2
    • 52949085789 scopus 로고    scopus 로고
    • Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs
    • Korn JM, Kuruvilla FG, McCarroll SA et al. Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs. Nat Genet 2008: 40: 1253-1260.
    • (2008) Nat Genet , vol.40 , pp. 1253-1260
    • Korn, J.M.1    Kuruvilla, F.G.2    McCarroll, S.A.3
  • 3
    • 34247877877 scopus 로고    scopus 로고
    • QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data
    • Colella S, Yau C, Taylor JM et al. QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data. Nucleic Acids Res 2007: 35: 2013-2025.
    • (2007) Nucleic Acids Res , vol.35 , pp. 2013-2025
    • Colella, S.1    Yau, C.2    Taylor, J.M.3
  • 4
    • 38149085456 scopus 로고    scopus 로고
    • The value of MUTYH testing in patients with early onset microsatellite stable colorectal cancer referred for hereditary nonpolyposis colon cancer syndrome testing
    • Riegert-Johnson DL, Johnson RA, Rabe KG et al. The value of MUTYH testing in patients with early onset microsatellite stable colorectal cancer referred for hereditary nonpolyposis colon cancer syndrome testing. Genet Test 2007: 11: 361-365.
    • (2007) Genet Test , vol.11 , pp. 361-365
    • Riegert-Johnson, D.L.1    Johnson, R.A.2    Rabe, K.G.3
  • 5
    • 34247569809 scopus 로고    scopus 로고
    • Recurrent 10q22-q23 deletions: a genomic disorder on 10q associated with cognitive and behavioral abnormalities
    • Balciuniene J, Feng N, Iyadurai K et al. Recurrent 10q22-q23 deletions: a genomic disorder on 10q associated with cognitive and behavioral abnormalities. Am J Hum Genet 2007: 80: 938-947.
    • (2007) Am J Hum Genet , vol.80 , pp. 938-947
    • Balciuniene, J.1    Feng, N.2    Iyadurai, K.3
  • 6
    • 79952769778 scopus 로고    scopus 로고
    • The phenotype of recurrent 10q22q23 deletions and duplications
    • van Bon BW, Balciuniene J, Fruhman G et al. The phenotype of recurrent 10q22q23 deletions and duplications. Eur J Hum Genet 2011: 19: 400-408.
    • (2011) Eur J Hum Genet , vol.19 , pp. 400-408
    • van Bon, B.W.1    Balciuniene, J.2    Fruhman, G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.