<i>CDKN1C</i> gene mutation causing familial Silver–Russell syndrome: A case report and review of literature-Reference-Cited by-同舟云学术

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CDKN1C gene mutation causing familial Silver–Russell syndrome: A case report and review of literature

Published:2023-07-06 Issue:19 Volume:11 Page:4655-4663
ISSN:2307-8960
Container-title:World Journal of Clinical Cases
language:
Short-container-title:World J Clin Cases

Author:

Li Jie,Chen Li-Na,He Hai-Lan

Publisher

Baishideng Publishing Group Inc.

Subject

General Medicine

Reference31 articles.

1. Deep exploration of a CDKN1C mutation causing a mixture of Beckwith-Wiedemann and IMAGe syndromes revealed a novel transcript associated with developmental delay

2. p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene.

3. Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann syndrome: an international consensus statement

4. Hypoglycemia in Beckwith-Wiedemann syndrome

5. Clinical features and natural history of Beckwith-Wiedemann syndrome: presentation of 74 new cases

Cited by 1 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. Approach to the Patient With Suspected Silver-Russell Syndrome;The Journal of Clinical Endocrinology & Metabolism;2024-06-18

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