Cargando…

Case report of a Li–Fraumeni syndrome-like phenotype with a de novo mutation in CHEK2: Erratum

Detalles Bibliográficos
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer Health 2016
Materias:	Erratum
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5266076/ https://www.ncbi.nlm.nih.gov/pubmed/31265670 http://dx.doi.org/10.1097/MD.0000000000005665

Ejemplares similares

Case report of a Li–Fraumeni syndrome-like phenotype with a de novo mutation in CHEK2
por: Zhuang, Xuehan, et al.
Publicado: (2016)

The contribution of CHEK2 to the TP53-negative Li-Fraumeni phenotype
por: Ruijs, Marielle WG, et al.
Publicado: (2009)

Is CHEK2 a moderate-risk breast cancer gene or the younger sister of Li-Fraumeni?
por: De Silva, Dilanka L, et al.
Publicado: (2020)

Li-Fraumeni Syndrome
por: Vogel, Wendy H.
Publicado: (2017)

A pedigree-based prediction model identifies carriers of deleterious de novo mutations in families with Li-Fraumeni syndrome
por: Gao, Fan, et al.
Publicado: (2020)

NSCLC With Synchronous EGFR Mutations in Li Fraumeni Syndrome: A Case Report
por: Marks, Jennifer A., et al.
Publicado: (2023)

Hematologic malignancies and Li–Fraumeni syndrome
por: Swaminathan, Mahesh, et al.
Publicado: (2019)

Rectal leiomyosarcoma as the initial phenotypic manifestation of Li–Fraumeni-like syndrome: a case report and review of the literature
por: Severino, Natalia Parisi, et al.
Publicado: (2022)

Li-Fraumeni syndrome: a case report from Italy.
por: Orjuela, M., et al.
Publicado: (1990)

A mouse model for Li-Fraumeni-Like Syndrome with cardiac angiosarcomas associated to POT1 mutations
por: Martínez, Paula, et al.
Publicado: (2022)

The first documentation of Li-Fraumeni syndrome in Korea.
por: Bang, Y. J., et al.
Publicado: (1995)

Pediatric Case of Li–Fraumeni Syndrome in Honduras
por: Martínez-Beckerat, R., et al.
Publicado: (2021)

Inhibiting the Priming for Cancer in Li-Fraumeni Syndrome
por: Pantziarka, Pan, et al.
Publicado: (2022)

Li-Fraumeni syndrome--a molecular and clinical review.
por: Varley, J. M., et al.
Publicado: (1997)

Li-Fraumeni Syndrome: A Rare Genetic Disorder
por: Tazin, Faria, et al.
Publicado: (2022)

Li‐Fraumeni versus Pseudo‐Li‐Fraumeni Syndrome: Key Insights for Interpreting Next‐Generation Sequencing Reports in Patients with Suspected Cancer Predisposition Syndromes
por: Sorscher, Steven, et al.
Publicado: (2017)

Li–Fraumeni syndrome in Tunisian carriers with different and rare tumor phenotype: genotype–phenotype correlation
por: Sassi, Hela, et al.
Publicado: (2022)

Does PTEN gene mutation play any role in Li-Fraumeni syndrome
por: Akouchekian, Mansoureh, et al.
Publicado: (2016)

The function of a heterozygous p53 mutation in a Li-Fraumeni syndrome patient
por: Li, Yang, et al.
Publicado: (2020)

A Case of Late-Onset Li-Fraumeni-like Syndrome with Unilateral Breast Cancer
por: Cho, Yonggeun, et al.
Publicado: (2013)

Li-Fraumeni-like syndrome associated with a large BRCA1 intragenic deletion
por: Silva, Amanda Gonçalves, et al.
Publicado: (2012)

Li Fraumeni syndrome, cancer and senescence: a new hypothesis
por: Pantziarka, Pan
Publicado: (2013)

PEComa in a Young Patient with Known Li-Fraumeni Syndrome
por: Neofytou, Kyriakos, et al.
Publicado: (2015)

The Features of Colorectal Tumors in a Patient with Li-Fraumeni Syndrome
por: Yoshida, Tsukasa, et al.
Publicado: (2017)

The Benefit and Burden of Cancer Screening in Li-Fraumeni Syndrome: A Case Report
por: Jhaveri, Ami P., et al.
Publicado: (2015)

The first pancreatic neuroendocrine tumor in Li-Fraumeni syndrome: a case report
por: Aversa, John G., et al.
Publicado: (2020)

A case report: invasive ductal carcinoma in mosaic Li-Fraumeni syndrome
por: Wenger, Danielle, et al.
Publicado: (2022)

Germline TP53 Mutation and Clinical Characteristics of Korean Patients With Li-Fraumeni Syndrome
por: Park, Kyoung-Jin, et al.
Publicado: (2016)

Erratum to “A De Novo Genome Assembly Algorithm for Repeats and Nonrepeats”
por: Lian, Shuaibin, et al.
Publicado: (2014)

A novel germline mutation of TP53 with breast cancer diagnosed as Li–Fraumeni syndrome
por: Kai, Masaya, et al.
Publicado: (2022)

A Case of Li-Fraumeni Associated Thymoma
por: Sivayoganathan, Thibacg, et al.
Publicado: (2022)

Genotype–phenotype associations within the Li-Fraumeni spectrum: a report from the German Registry
por: Penkert, Judith, et al.
Publicado: (2022)

Primed for cancer: Li Fraumeni Syndrome and the pre-cancerous niche
por: Pantziarka, Pan
Publicado: (2015)

Prostate Cancer and Li-Fraumeni Syndrome: Implications for Screening and Therapy
por: Spees, Colleen K., et al.
Publicado: (2015)

Genetic and functional analysis of a Li Fraumeni syndrome family in China
por: Hu, Huaying, et al.
Publicado: (2016)

Maxillary mesenchymal chondrosarcoma leading to a diagnosis of Li-Fraumeni syndrome
por: Ventura, Eduardo, et al.
Publicado: (2020)

Distinct NSCLC EGFR Variants in a Family With Li-Fraumeni Syndrome: Case Report
por: Edmondson, Shelby, et al.
Publicado: (2022)

Constitutional p53 mutation in a non-Li-Fraumeni cancer family.
por: Prosser, J., et al.
Publicado: (1992)

Molecular characteristics of endometrial cancer coexisting with peritoneal malignant mesothelioma in Li-Fraumeni-like syndrome
por: Chao, Angel, et al.
Publicado: (2015)

Heterogeneity of Li-Fraumeni Syndrome links to unequal gain-of-function effects of p53 mutations
por: Xu, Jie, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_c5gbte8b3mq6icqenp1o4gfmip