Risk of breast cancer not increased in translocation 11;22 carriers: analysis of 80 pedigrees.
作者信息
Carter Melissa T, Barrowman Nicholas J, St Pierre Stephanie A, Emanuel Beverly S, Boycott Kym M
机构信息
Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Canada.
出版信息
Am J Med Genet A. 2010 Jan;152A(1):212-4. doi: 10.1002/ajmg.a.33166.
Abstract
摘要
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Risk of breast cancer not increased in translocation 11;22 carriers: analysis of 80 pedigrees.11号与22号染色体易位携带者患乳腺癌风险未增加：对80个家系的分析
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Phenotypic delineation of Emanuel syndrome (supernumerary derivative 22 syndrome): Clinical features of 63 individuals.Emanuel综合征（额外衍生22号染色体综合征）的表型描述：63例个体的临床特征
Am J Med Genet A. 2009 Aug;149A(8):1712-21. doi: 10.1002/ajmg.a.32957.
2
High incidence of familial breast cancer segregates with constitutional t(11;22)(q23;q11).家族性乳腺癌的高发病率与染色体组型t(11;22)(q23;q11)相关。
Genes Chromosomes Cancer. 2006 Oct;45(10):945-9. doi: 10.1002/gcc.20358.
3
A unique case of der(11)t(11;22),-22 arising from 3:1 segregation of a maternal t(11;22) in a family with co-segregation of the translocation and breast cancer.在一个易位与乳腺癌共分离的家族中，出现了一例源于母亲t(11;22) 3:1分离的der(11)t(11;22),-22独特病例。
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Does this patient have a family history of cancer? An evidence-based analysis of the accuracy of family cancer history.该患者有癌症家族病史吗？一项关于家族癌症病史准确性的循证分析。
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Candidate tumour suppressor genes at 11q23-q24 in breast cancer: evidence of alterations in PIG8, a gene involved in p53-induced apoptosis.乳腺癌中位于11q23 - q24的候选抑癌基因：参与p53诱导凋亡的PIG8基因改变的证据
Oncogene. 2001 Nov 22;20(53):7753-60. doi: 10.1038/sj.onc.1204993.
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Accuracy of family history of cancer: clinical genetic implications.癌症家族史的准确性：临床遗传学意义。
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Accuracy of case-reported family history of melanoma in Queensland, Australia.
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