Contiguous gene deletion of chromosome 2p16.3-p21 as a cause of Lynch syndrome-Reference-Cited by-同舟云学术

Contiguous gene deletion of chromosome 2p16.3-p21 as a cause of Lynch syndrome

Published:2017-05-29 Issue:1 Volume:17 Page:71-77
ISSN:1389-9600
Container-title:Familial Cancer
language:en
Short-container-title:Familial Cancer

Author:

Salo-Mullen Erin E.,Lynn Patricio B.,Wang Lu,Walsh Michael,Gopalan Anuradha,Shia Jinru,Tran Christina,Man Fung Ying,McBride Sean,Schattner Mark,Zhang Liying,Weiser Martin R.,Stadler Zsofia K.

Funder

National Cancer Institute

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Genetics (clinical),Oncology,Genetics

Link

http://link.springer.com/article/10.1007/s10689-017-0006-x/fulltext.html

Reference12 articles.

1. Lynch HT, Lynch PM, Lanspa SJ, Snyder CL, Lynch JF, Boland CR (2009) Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications. Clin Genet 76(1):1–18

2. Nussbaum RL, McInnes RR, Williard HF (2004) Thompson and Thompson genetics in medicine, 6th edn. Saunders/Elsevier, Philadelphia, pp 164–165

3. Adams SA, Coppinger J, Saitta SC, Stroud T, Kandamurugu M, Fan Z, Ballif BC, Shaffer LG, Bejjani BA (2009) Impact of genotype-first diagnosis: the detection of microdeletion and microduplication syndromes with cancer predisposition by aCGH. Genet Med 11(5):314–322

4. Herrera L, Kakati S, Gibas L, Pietrzak K, Sandberg AA (1986) Gardner syndrome in a man with an interstitial deletion of 5q. Am J Med Genet 25(3):473–476

5. Raedle J, Friedl W, Engels H, Koenig R, Trojan J, Zeuzem S (2001) A de novo deletion of chromosome 5q causing familial adenomatous polyposis, dysmorphic features, and mild mental retardation. Am J Gastroenterol 96(10):3016–3020

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