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Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10,000 individuals.
J Clin Oncol. 2002 Mar 15;20(6):1480-90. doi: 10.1200/JCO.2002.20.6.1480.
J Clin Oncol. 2002.
PMID: 11896095
BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testing.
Shattuck-Eidens D, Oliphant A, McClure M, McBride C, Gupte J, Rubano T, Pruss D, Tavtigian SV, Teng DH, Adey N, Staebell M, Gumpper K, Lundstrom R, Hulick M, Kelly M, Holmen J, Lingenfelter B, Manley S, Fujimura F, Luce M, Ward B, Cannon-Albright L, Steele L, Offit K, Thomas A, et al.
Shattuck-Eidens D, et al.
JAMA. 1997 Oct 15;278(15):1242-50.
JAMA. 1997.
PMID: 9333265
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Hereditary susceptibility to breast cancer: significance of age of onset in family history and contribution of BRCA1 and BRCA2.
Frank TS, Deffenbaugh AM, Hulick M, Gumpper K.
Frank TS, et al.
Dis Markers. 1999 Oct;15(1-3):89-92. doi: 10.1155/1999/291023.
Dis Markers. 1999.
PMID: 10595259
Free PMC article.
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Microsatellite deletion mapping on chromosome 10q and mutation analysis of MMAC1, FAS, and MXI1 in human glioblastoma multiforme.
Fults D, Pedone CA, Thompson GE, Uchiyama CM, Gumpper KL, Iliev D, Vinson VL, Tavtigian SV, Perry WL 3rd.
Fults D, et al. Among authors: gumpper kl.
Int J Oncol. 1998 Apr;12(4):905-10. doi: 10.3892/ijo.12.4.905.
Int J Oncol. 1998.
PMID: 9499454
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MMAC1/PTEN mutations in primary tumor specimens and tumor cell lines.
Teng DH, Hu R, Lin H, Davis T, Iliev D, Frye C, Swedlund B, Hansen KL, Vinson VL, Gumpper KL, Ellis L, El-Naggar A, Frazier M, Jasser S, Langford LA, Lee J, Mills GB, Pershouse MA, Pollack RE, Tornos C, Troncoso P, Yung WK, Fujii G, Berson A, Steck PA, et al.
Teng DH, et al. Among authors: gumpper kl.
Cancer Res. 1997 Dec 1;57(23):5221-5.
Cancer Res. 1997.
PMID: 9393738
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