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Hereditary cancer AND (genetic OR genomic) AND review - PubMed - NCBI

Hereditary cancer AND (genetic OR genomic) AND review - PubMed - NCBI

Hereditary Cancer

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[Hereditary colorectal cancer].
Hindi Muñiz N, Lamarca Lete A, Feliú Batlle J.
Med Clin (Barc). 2012 Mar 3;138(5):220-3. doi: 10.1016/j.medcli.2011.09.019. Epub 2011 Nov 16. Review. Spanish.

PMID:
 
22093404
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An overview of hereditary breast and ovarian cancer syndrome.
Smith EC.
J Midwifery Womens Health. 2012 Nov-Dec;57(6):577-584. doi: 10.1111/j.1542-2011.2012.00199.x. Epub 2012 Oct 10. Review.

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Cancer genomics and inherited risk.
Stadler ZK, Schrader KA, Vijai J, Robson ME, Offit K.
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Cancer syndromes and therapy by stop-codon readthrough.
Bordeira-Carriço R, Pêgo AP, Santos M, Oliveira C.
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[The genome and cancer treatment].
Nielsen FC, Lassen U.
Ugeskr Laeger. 2014 Nov 10;176(46). pii: V07140419. Review. Danish.

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Whartenby KA.
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Integration of genomics in cancer care.
Santos EM, Edwards QT, Floria-Santos M, Rogatto SR, Achatz MI, MacDonald DJ.
J Nurs Scholarsh. 2013 Mar;45(1):43-51. doi: 10.1111/j.1547-5069.2012.01465.x. Epub 2013 Jan 7. Review.

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Whole-genome and whole-exome sequencing in hereditary cancer: impact on genetic testing and counseling.
O'Daniel JM, Lee K.
Cancer J. 2012 Jul-Aug;18(4):287-92. doi: 10.1097/PPO.0b013e318262467e. Review.

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E-cadherin germline mutation carriers: clinical management and genetic implications.
Corso G, Figueiredo J, Biffi R, Trentin C, Bonanni B, Feroce I, Serrano D, Cassano E, Annibale B, Melo S, Seruca R, De Lorenzi F, Ferrara F, Piagnerelli R, Roviello F, Galimberti V.
Cancer Metastasis Rev. 2014 Dec;33(4):1081-94. doi: 10.1007/s10555-014-9528-y. Review.

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Genome-wide sequencing to identify the cause of hereditary cancer syndromes: with examples from familial pancreatic cancer.
Roberts NJ, Klein AP.
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Communication and technology in genetic counseling for familial cancer.
Lynch HT, Snyder C, Stacey M, Olson B, Peterson SK, Buxbaum S, Shaw T, Lynch PM.
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[Colorectal cancer (CCR): genetic and molecular alterations].
Juárez-Vázquez CI, Rosales-Reynoso MA.
Gac Med Mex. 2014 Mar-Apr;150(2):154-64. Review. Spanish.

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Beyond BRCA1 and BRCA2.
King-Spohn K, Pilarski R.
Curr Probl Cancer. 2014 Nov-Dec;38(6):235-48. doi: 10.1016/j.currproblcancer.2014.10.004. Epub 2014 Nov 1.

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Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the U.S. Multi-Society Task Force on Colorectal Cancer.
Giardiello FM, Allen JI, Axilbund JE, Boland CR, Burke CA, Burt RW, Church JM, Dominitz JA, Johnson DA, Kaltenbach T, Levin TR, Lieberman DA, Robertson DJ, Syngal S, Rex DK; American Society for Gastrointestinal Endoscopy.
Gastrointest Endosc. 2014 Aug;80(2):197-220. doi: 10.1016/j.gie.2014.06.006. Review. No abstract available.

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[Hepatic involvement in hereditary alpha-1-antitrypsin deficiency].
Lachaux A, Dumortier J.
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Impact of tumor sequencing on the use of anticancer drugs.
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[DNA methylation defects in sporadic and hereditary colorectal cancer].
Xicola RM, Llor X.
Gastroenterol Hepatol. 2012 Aug-Sep;35(7):480-7. doi: 10.1016/j.gastrohep.2012.01.010. Epub 2012 Mar 27. Review. Spanish.

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[Genetic diagnosis for cancer--tumorigenesis and genetic alterations].
Maekawa M, Sugano K.
Rinsho Byori. 2000 Feb;48(2):143-8. Review. Japanese.

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Hereditary ovarian cancer: recent molecular insights and their impact on screening strategies.
Long KC, Kauff ND.
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Genetic counselling for hereditary predisposition to ovarian and breast cancer.
Mackay J, Szecsei CM.
Ann Oncol. 2010 Oct;21 Suppl 7:vii334-8. doi: 10.1093/annonc/mdq365. Review.

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