Four new cases of double heterozygosity for BRCA1 and BRCA2 gene mutations: clinical, pathological, and family characteristics
暂无分享,去创建一个
P. Radice | S. Manoukian | V. Pensotti | A. Santoro | B. Peissel | M. Barile | A. Benski | D. Zaffaroni | G. Masci | M. Zuradelli | F. Mariette | U. Cavallari
[1] F. Sera,et al. Founder mutations account for the majority of BRCA1-attributable hereditary breast/ovarian cancer cases in a population from Tuscany, Central Italy , 2009, Breast Cancer Research and Treatment.
[2] P. Radice,et al. Germline mutations of TP53 and BRCA2 genes in breast cancer/sarcoma families. , 2007, European journal of cancer.
[3] A. Musolino,et al. A breast cancer patient from Italy with germline mutations in both the BRCA1 and BRCA2 genes , 2005, Breast Cancer Research and Treatment.
[4] R. Eeles,et al. Phenotypic expression of double heterozygosity for BRCA1 and BRCA2 germline mutations , 2005, Journal of Medical Genetics.
[5] D. Carter,et al. Prevalence of BRCA1 and BRCA2 mutations in women diagnosed with ductal carcinoma in situ. , 2005, JAMA.
[6] B. Haffty,et al. Incidence of BRCA1 and BRCA2 mutations in young Korean breast cancer patients. , 2004, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[7] J. Godino,et al. A breast cancer family from Spain with germline mutations in both the BRCA1 and BRCA2 genes , 2002, Journal of medical genetics.
[8] D. Sgroi,et al. Selective loss of heterozygosity in multiple breast cancers from a carrier of mutations in both BRCA1 and BRCA2. , 2002, Cancer research.
[9] Sean V Tavtigian,et al. Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10,000 individuals. , 2002, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[10] E. Steegers,et al. Paternal contribution to the risk for pre-eclampsia , 2002, Journal of medical genetics.
[11] P. Radice,et al. Evidence of a founder mutation of BRCA1 in a highly homogeneous population from southern Italy with breast/ovarian cancer , 2001, Human mutation.
[12] K. Phillips. Immunophenotypic and pathologic differences between BRCA1 and BRCA2 hereditary breast cancers. , 2000, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[13] S. Narod,et al. An unaffected individual from a breast/ovarian cancer family with germline mutations in both BRCA1 and BRCA2 , 2000, Clinical genetics.
[14] G. Giles,et al. De novo BRCA1 mutation in a patient with breast cancer and an inherited BRCA2 mutation. , 1999, American journal of human genetics.
[15] S. Seal,et al. Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer. , 1999, Journal of the National Cancer Institute.
[16] S Wacholder,et al. The prevalence of common BRCA1 and BRCA2 mutations among Ashkenazi Jews. , 1999, American journal of human genetics.
[17] R. Gershoni-baruch,et al. Double heterozygotes for the Ashkenazi founder mutations in BRCA1 and BRCA2 genes. , 1998, American journal of human genetics.
[18] J. Boyd,et al. Germline mutations of the BRCA1 and BRCA2 genes in a breast and ovarian cancer patient. , 1998, Gynecologic oncology.
[19] H. Yokozaki,et al. [Hereditary non-polyposis colorectal cancer]. , 1998, Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine.
[20] S. Narod,et al. A breast cancer patient of Scottish descent with germ-line mutations in BRCA1 and BRCA2. , 1998, American journal of human genetics.
[21] R. Gershoni-baruch,et al. Co-segregation of BRCA1 185delAG mutation and BRCA2 6174delT in one single family. , 1997, European journal of cancer.
[22] M. Skolnick,et al. BRCA1 germline mutational spectrum in Italian families from Tuscany: a high frequency of novel mutations. , 1996, Oncogene.
[23] Kenneth Offit,et al. The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1% , 1996, Nature Genetics.
[24] Alfred A. Boyd,et al. Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2 , 1996, Nature Genetics.
[25] F. Collins,et al. The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals , 1995, Nature Genetics.
[26] I. Winship,et al. Familial breast cancer: double heterozygosity for BRCA1 and BRCA2 mutations with differing phenotypes , 2007, Familial Cancer.
[27] S. Loader,et al. Deleterious mutations of both BRCA1 and BRCA2 in three siblings. , 1998, Genetic testing.
[28] B. Ponder,et al. A breast/ovarian cancer patient with germline mutations in both BRCA1 and BRCA2 , 1997, Nature Genetics.