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1
Risk of breast cancer not increased in translocation 11;22 carriers: analysis of 80 pedigrees.
Am J Med Genet A. 2010 Jan;152A(1):212-4. doi: 10.1002/ajmg.a.33166.
2
High incidence of familial breast cancer segregates with constitutional t(11;22)(q23;q11).
Genes Chromosomes Cancer. 2006 Oct;45(10):945-9. doi: 10.1002/gcc.20358.
4
Mortality and cancer incidence in carriers of constitutional t(11;22)(q23;q11) translocations: A prospective study.
Int J Cancer. 2019 Sep 15;145(6):1493-1498. doi: 10.1002/ijc.32031. Epub 2019 Jan 11.
5
Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22).
Am J Hum Genet. 2000 Sep;67(3):763-8. doi: 10.1086/303054. Epub 2000 Jul 20.
6
Involvement of 3:1 disjunction in the common reciprocal translocation t(11;22) (q23.3;q11.2).
Hum Genet. 1992 Sep-Oct;90(1-2):191-2. doi: 10.1007/BF00210779.
8
Unusual segregation in a family with a 11/21 translocation.
Clin Genet. 1988 Jun;33(6):449-53. doi: 10.1111/j.1399-0004.1988.tb03479.x.
9
A 7 Mb region within 11q13 may contain a high penetrance gene for breast cancer.
Breast Cancer Res Treat. 2009 Nov;118(1):151-9. doi: 10.1007/s10549-009-0317-1. Epub 2009 Feb 10.
10
The importance of aneuploidy screening in reciprocal translocation carriers.
Reproduction. 2006 Jun;131(6):1025-35. doi: 10.1530/rep.1.01063.

引用本文的文献

1
Mortality and cancer incidence in carriers of constitutional t(11;22)(q23;q11) translocations: A prospective study.
Int J Cancer. 2019 Sep 15;145(6):1493-1498. doi: 10.1002/ijc.32031. Epub 2019 Jan 11.
2
The effect of translocation-induced nuclear reorganization on gene expression.
Genome Res. 2010 May;20(5):554-64. doi: 10.1101/gr.103622.109. Epub 2010 Mar 8.

本文引用的文献

2
High incidence of familial breast cancer segregates with constitutional t(11;22)(q23;q11).
Genes Chromosomes Cancer. 2006 Oct;45(10):945-9. doi: 10.1002/gcc.20358.
6
Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22).
Am J Hum Genet. 2000 Sep;67(3):763-8. doi: 10.1086/303054. Epub 2000 Jul 20.
7
Accuracy of family history of cancer: clinical genetic implications.
Eur J Hum Genet. 2000 Mar;8(3):181-6. doi: 10.1038/sj.ejhg.5200441.
9
Alterations of the PPP2R1B gene in human lung and colon cancer.
Science. 1998 Oct 9;282(5387):284-7. doi: 10.1126/science.282.5387.284.
10
Accuracy of case-reported family history of melanoma in Queensland, Australia.
Melanoma Res. 1996 Aug;6(4):313-7. doi: 10.1097/00008390-199608000-00006.

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