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Journal Abstract Search

81 related items for PubMed ID: 9562970

  • 1. 11q13 allelotype analysis in 27 northern American MEN1 kindreds identifies two distinct founder chromosomes.
    Emmert-Buck MR, Debelenko LV, Agarwal S, Kester MB, Manickam P, Zhuang Z, Guru SC, Olufemi SE, Burns AL, Chandrasekharappa SC, Lubensky IA, Liotta LA, Skarulis MC, Spiegel AM, Marx SJ, Collins FS.
    Mol Genet Metab; 1998 Feb; 63(2):151-5. PubMed ID: 9562970
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  • 2. Common ancestral mutation in the MEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1Burin) in four kindreds from Newfoundland.
    Olufemi SE, Green JS, Manickam P, Guru SC, Agarwal SK, Kester MB, Dong Q, Burns AL, Spiegel AM, Marx SJ, Collins FS, Chandrasekharappa SC.
    Hum Mutat; 1998 Feb; 11(4):264-9. PubMed ID: 9554741
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  • 3. Haplotype analysis defines a minimal interval for the multiple endocrine neoplasia type 1 (MEN1) gene.
    Debelenko LV, Emmert-Buck MR, Manickam P, Kester M, Guru SC, DiFranco EM, Olufemi SE, Agarwal S, Lubensky IA, Zhuang Z, Burns AL, Spiegel AM, Liotta LA, Collins FS, Marx SJ, Chandrasekharappa SC.
    Cancer Res; 1997 Mar 15; 57(6):1039-42. PubMed ID: 9067266
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  • 4. Analysis of recurrent germline mutations in the MEN1 gene encountered in apparently unrelated families.
    Agarwal SK, Debelenko LV, Kester MB, Guru SC, Manickam P, Olufemi SE, Skarulis MC, Heppner C, Crabtree JS, Lubensky IA, Zhuang Z, Kim YS, Chandrasekharappa SC, Collins FS, Liotta LA, Spiegel AM, Burns AL, Emmert-Buck MR, Marx SJ.
    Hum Mutat; 1998 Mar 15; 12(2):75-82. PubMed ID: 9671267
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  • 7. Multiple endocrine neoplasia type 1 (MEN1): LOH studies in a affected family and in sporadic cases.
    Valdes N, Alvarez V, Diaz-Cadorniga F, Aller J, Villazon F, Garcia I, Herrero A, Coto E.
    Anticancer Res; 1998 Mar 15; 18(4A):2685-9. PubMed ID: 9703929
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  • 8. Isolated familial somatotropinomas: clinical and genetic considerations.
    Frohman LA.
    Trans Am Clin Climatol Assoc; 2003 Mar 15; 114():165-77. PubMed ID: 12813918
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  • 9. Sequence analysis and transcript expression of the MEN1 gene in sporadic pituitary tumours.
    Farrell WE, Simpson DJ, Bicknell J, Magnay JL, Kyrodimou E, Thakker RV, Clayton RN.
    Br J Cancer; 1999 Apr 15; 80(1-2):44-50. PubMed ID: 10389976
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  • 11. Genetic alterations on 3p, 11q13, and 18q in nonfamilial and MEN 1-associated pancreatic endocrine tumors.
    Hessman O, Lindberg D, Einarsson A, Lillhager P, Carling T, Grimelius L, Eriksson B, Akerström G, Westin G, Skogseid B.
    Genes Chromosomes Cancer; 1999 Nov 15; 26(3):258-64. PubMed ID: 10502325
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  • 12. Eighteen new polymorphic markers in the multiple endocrine neoplasia type 1 (MEN1) region.
    Manickam P, Guru SC, Debelenko LV, Agarwal SK, Olufemi SE, Weisemann JM, Boguski MS, Crabtree JS, Wang Y, Roe BA, Lubensky IA, Zhuang Z, Kester MB, Burns AL, Spiegel AM, Marx SJ, Liotta LA, Emmert-Buck MR, Collins FS, Chandrasekharappa SC.
    Hum Genet; 1997 Nov 15; 101(1):102-8. PubMed ID: 9385379
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  • 13. Cytogenetic and molecular analyses of multiple endocrine neoplasias of the MEN1 syndrome.
    Pourani J, Kaserer K, Pfragner R.
    Int J Oncol; 2002 May 15; 20(5):971-6. PubMed ID: 11956591
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  • 15. Predictive testing for multiple endocrine neoplasia type 1 using DNA polymorphisms.
    Larsson C, Shepherd J, Nakamura Y, Blomberg C, Weber G, Werelius B, Hayward N, Teh B, Tokino T, Seizinger B.
    J Clin Invest; 1992 Apr 15; 89(4):1344-9. PubMed ID: 1348254
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  • 16. Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping.
    Kibar Z, Dubé MP, Powell J, McCuaïg C, Hayflick SJ, Zonana J, Hovnanian A, Radhakrishna U, Antonarakis SE, Benohanian A, Sheeran AD, Stephan ML, Gosselin R, Kelsell DP, Christianson AL, Fraser FC, Der Kaloustian VM, Rouleau GA.
    Eur J Hum Genet; 2000 May 15; 8(5):372-80. PubMed ID: 10854098
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  • 19. The European Consortium on MEN1. Linkage disequilibrium studies in multiple endocrine neoplasia type 1 (MEN1).
    Hum Genet; 1997 Oct 15; 100(5-6):657-65. PubMed ID: 9341888
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