H19 gene polymorphisms and Wilms tumor risk in Chinese children: a four‐center case‐control study

Author:

Li Wenya1ORCID,Hua Rui‐Xi23,Wang Mi3,Zhang Da1,Zhu Jinhong34,Zhang Songyang1,Yang Yang1,Cheng Jiwen5,Zhou Haixia6,Zhang Jiao1,He Jing3ORCID

Affiliation:

1. Department of Pediatric Surgery The First Affiliated Hospital of Zhengzhou University Zhengzhou China

2. Department of Oncology The First Affiliated Hospital of Sun Yat‐sen University Guangzhou China

3. Department of Pediatric Surgery Guangzhou Institute of Pediatrics Guangdong Provincial Key Laboratory of Research in Structural Birth Defect Disease Guangzhou Women and Children's Medical Center Guangzhou Medical University Guangzhou China

4. Department of Clinical Laboratory Biobank Harbin Medical University Cancer Hospital Harbin China

5. Department of Pediatric Surgery the Second Affiliated Hospital of Xi'an Jiaotong University Xi'an China

6. Department of Hematology The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University Wenzhou China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Reference64 articles.

1. The product of the imprinted H19 gene is an oncofetal RNA.

2. Recent incidences and trends of childhood malignant solid tumors in Shanghai, 2002–2010;Bao P. P.;Zhonghua Er Ke Za Zhi,2013

3. Letter to the Editor: Commentary on "Is it possible to predict the origin of epithelial cells? ‐ A comparison of secondary transfer of skin epithelial cells versus vaginal mucous membrane cells by direct contact M.M. Bouzga et al;Biedermann A.;Science & Justice: Journal of the Forensic Science Society,2020

4. Epidemiologic Features of Wilms Tumor

5. Ethnic Variation in the Incidence, Diagnosis, Prognosis, and Follow-up of Children With Wilms' Tumor

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