A spectrum of TP63-related disorders with eight affected individuals in five unrelated families-Reference-Cited by-同舟云学术

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A spectrum of TP63-related disorders with eight affected individuals in five unrelated families

Published:2024-04 Issue: Volume:68 Page:104911
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Soğukpınar Merve^ORCID,Utine Gülen Eda,Boduroğlu Koray,Şimşek-Kiper Pelin Özlem

Publisher

Elsevier BV

Reference24 articles.

1. Two case reports with literature review of the EEC syndrome: clinical presentation and management;Augello;Case Rep. Plast Surg. Hand Surg.,2015

2. Genome-wide association study in craniosynostosis condition using innovative systematic bioinformatic analysis tools and techniques: future prospective and clinical practice;Barik;J. Pediatr. Neurosci.,2018

3. The p63 gene in EEC and other syndromes;Brunner;J. Med. Genet.,2002

4. Twenty-four cases of the EEC syndrome: clinical presentation and management;Buss;J. Med. Genet.,1995

5. Solution structure of a conserved C-terminal domain of p73 with structural homology to the SAM domain;Chi;EMBO J.,1999

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