KID Syndrome: Report of a Scandinavian Patient with Connexin‐26 Gene Mutation-Reference-Cited by-同舟云学术

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KID Syndrome: Report of a Scandinavian Patient with Connexin‐26 Gene Mutation

Published:2005-03-01 Issue:2 Volume:85 Page:152-155
ISSN:0001-5555
Container-title:Acta Dermato-Venereologica
language:
Short-container-title:Acta Dermato-Venereologica

Author:

Bygum Anette,Betz Regina,Kragballe Knud,Steiniche Torben,Peeters Nils,Wuyts Wim,Nöthen Markus

Publisher

Medical Journals Sweden AB

Subject

Dermatology,General Medicine

Cited by 22 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. Posterior Cranial Fossa Malformation and Vascular Dysplasia in GJB2 Gene Mutation;Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques;2023-09-08

2. Of Mycelium and Men: Inherent Human Susceptibility to Fungal Diseases;Pathogens;2023-03-14

3. Keratitis‐ichthyosis‐deafness syndrome: A comprehensive review of cutaneous and systemic manifestations;Pediatric Dermatology;2022-11-29

4. A Rare Case of KID Syndrome: The Use of Hydrosurgery and Strategies for Antiseptic Wound Care;Advances in Skin & Wound Care;2019-10

5. Skin Cancer Associated Genodermatoses: A Literature Review;Acta Dermato Venereologica;2019

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