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Volumn 79, Issue 3, 2006, Pages 593-596

Deletion of PTEN and BMPR1A on chromosome 10q23 is not always associated with juvenile polyposis of infancy [1]

Author keywords

[No Author keywords available]

Indexed keywords

BMPR1A GENE; CASE REPORT; CHILD; CHROMOSOME 10Q; DISEASE ASSOCIATION; FEMALE; GENE; GENE DELETION; HUMAN; JUVENILE POLYP; JUVENILE POLYPOSIS OF INFANCY; LETTER; MOLECULAR CLONING; PRIORITY JOURNAL; PTEN GENE; TUMOR SUPPRESSOR GENE;

EID: 33748669256     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/507151     Document Type: Letter
Times cited : (38)

References (10)
  • 2
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    • Hereditary polypoid diseases of the gastrointestinal tract: A working classification
    • Sachatello CR, Griffen WO Jr (1975) Hereditary polypoid diseases of the gastrointestinal tract: a working classification. Am J Surg 129:198-203
    • (1975) Am J Surg , vol.129 , pp. 198-203
    • Sachatello, C.R.1    Griffen Jr., W.O.2
  • 3
    • 3342929410 scopus 로고    scopus 로고
    • Genetic conditions associated with intestinal juvenile polyps
    • Merg A, Howe JR (2004) Genetic conditions associated with intestinal juvenile polyps. Am J Med Genet C Semin Med Genet 129:44-55
    • (2004) Am J Med Genet C Semin Med Genet , vol.129 , pp. 44-55
    • Merg, A.1    Howe, J.R.2
  • 4
    • 0031914727 scopus 로고    scopus 로고
    • Deletion 10q23.2-q23.33 in a patient with gastrointestinal juvenile polyposis and other features of a Cowden-like syndrome
    • Tsuchiya KD, Wiesner G, Cassidy SB, Limwongse C, Boyle JT, Schwartz S (1998) Deletion 10q23.2-q23.33 in a patient with gastrointestinal juvenile polyposis and other features of a Cowden-like syndrome. Genes Chromosomes Cancer 21:113-118
    • (1998) Genes Chromosomes Cancer , vol.21 , pp. 113-118
    • Tsuchiya, K.D.1    Wiesner, G.2    Cassidy, S.B.3    Limwongse, C.4    Boyle, J.T.5    Schwartz, S.6
  • 6
    • 0042316755 scopus 로고    scopus 로고
    • PTEN: One gene, many syndromes
    • Eng C (2003) PTEN: one gene, many syndromes. Hum Mutat 22:183-198
    • (2003) Hum Mutat , vol.22 , pp. 183-198
    • Eng, C.1
  • 7
    • 0036798926 scopus 로고    scopus 로고
    • DiGeorge syndrome: The use of model organisms to dissect complex genetics
    • Baldini A (2002) DiGeorge syndrome: the use of model organisms to dissect complex genetics. Hum Mol Genet 11:2363-2369
    • (2002) Hum Mol Genet , vol.11 , pp. 2363-2369
    • Baldini, A.1
  • 8
    • 0042632658 scopus 로고    scopus 로고
    • Spectrum of clinical variability in familial deletion 22q11.2: From full manifestation to extremely mild clinical anomalies
    • Digilio MC, Angioni A, De Santis M, Lombardo A, Giannotti A, Dallapiccola B, Marino B (2003) Spectrum of clinical variability in familial deletion 22q11.2: from full manifestation to extremely mild clinical anomalies. Clin Genet 63:308-313
    • (2003) Clin Genet , vol.63 , pp. 308-313
    • Digilio, M.C.1    Angioni, A.2    De Santis, M.3    Lombardo, A.4    Giannotti, A.5    Dallapiccola, B.6    Marino, B.7
  • 9
    • 0029033305 scopus 로고
    • Monozygotic twins with chromosome 22q11 deletion and discordant phenotype
    • Goodship J, Cross I, Scambler P, Burn J (1995) Monozygotic twins with chromosome 22q11 deletion and discordant phenotype. J Med Genet 32:746-748
    • (1995) J Med Genet , vol.32 , pp. 746-748
    • Goodship, J.1    Cross, I.2    Scambler, P.3    Burn, J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.