A Case report: Co-occurrence of IMAGe syndrome and Rhabdomyosarcoma-Reference-Cited by-同舟云学术

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A Case report: Co-occurrence of IMAGe syndrome and Rhabdomyosarcoma

Published:2021-08 Issue: Volume:256-257 Page:100-105
ISSN:2210-7762
Container-title:Cancer Genetics
language:en
Short-container-title:Cancer Genetics

Author:

Bolomiti Maria^ORCID,Båtnes-Pedersen Erik,Telman Gabriela,Januszkiewicz-Lewandowska Danuta

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology

Reference18 articles.

1. IMAGe syndrome;Bennett,2020

2. IMAGe, a new clinical association of intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies;Vilain;J Clin Endocrinol Metab,1999

3. Familial occurrence of the IMAGe association: additional clinical variants and a proposed mode of inheritance;Bergada;J Clin Endocrinol Metab,2005

4. Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndrome;Arboleba;Nat Genet,2012

5. Silencing of CDKN1C (p75KIP2) is associated with hypomethylation at KvDMR1 in Beck-Wiedemann syndrome;Diaz-Meyer;J Med Genet,2003

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Clinical Spectrum and Tumour Risk Analysis in Patients with Beckwith-Wiedemann Syndrome Due to CDKN1C Pathogenic Variants;Cancers;2022-08-05

2. An Update on Genetics of Adrenal Gland and Associated Disorders;Endocrines;2022-04-13

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