Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations-Reference-Cited by-同舟云学术

Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations

Published:2010-06-24 Issue:4 Volume:9 Page:625-633
ISSN:1389-9600
Container-title:Familial Cancer
language:en
Short-container-title:Familial Cancer

Author:

Yang Xiaohong Rose,Liang Xueying,Pfeiffer Ruth M.,Wheeler William,Maeder Dennis,Burdette Laurie,Yeager Meredith,Chanock Stephen,Tucker Margaret A.,Goldstein Alisa M.

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Genetics(clinical),Oncology,Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10689-010-9356-3.pdf

Reference49 articles.

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3. Goldstein AM (2004) Familial melanoma, pancreatic cancer and germline CDKN2A mutations. Hum Mutat 23(6):630

4. Rakosy Z, Vizkeleti L, Ecsedi S et al (2008) Characterization of 9p21 copy number alterations in human melanoma by fluorescence in situ hybridization. Cancer Genet Cytogenet 182(2):116–121

5. Zhu G, Montgomery GW, James MR et al (2007) A genome-wide scan for naevus count: linkage to CDKN2A and to other chromosome regions. Eur J Hum Genet 15(1):94–102

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