A challenging clinical case. Patient with multiple primary neoplasias and no family history of cancer: Richter syndrome versus Familial Melanoma plus Li-Fraumeni syndrome

被引：0
|
作者：
Castillejo, A. [1 ,2 ]
Castillejo, M. I. [1 ,2 ]
Sanchez-Heras, A. B. [3 ]
Garrigos, N. [4 ]
Capella, G. [5 ]
Lazaro, C. [5 ]
Serra, E. [6 ]
Soto, J. L. [1 ,7 ]
机构：
[1] Elche Univ Hosp, Mol Genet Unit, Elche, Spain
[2] Fdn Promot Biomed & Sanitary Res FISABIO, Valencia, Spain
[3] Elche Univ Hosp, Genet Counseling Canc Unit, Elche, Spain
[4] Alicante Immunol Ctr, San Juan, Spain
[5] Catalan Inst Oncol, Joint Program Hereditary Canc, Hereditary Canc Program, IDIBELL Campus, Lhospitalet De Llobregat, Spain
[6] Germans Trias & Pujol Res Inst IGTP, Program Predict & Personalized Med Canc PMPPC, Hereditary Canc Grp, Can Ruti Campus, Badalona, Spain
[7] ISABIAL FISABIO Fdn, Alicante Inst Hlth & Biomed Res, Alicante, Spain
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2019年 / 27卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
P12.182B
引用
收藏
页码：462 / 463
页数：2
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