THE PATTERN OF INHERITANCE IN KID SYNDROME
Author:
Affiliation:
1. Milan, Italy
Publisher
Wiley
Subject
Dermatology,Pediatrics, Perinatology and Child Health
Reference5 articles.
1. Keratitis, ichthyosis, and deafness (KID) syndrome in half sibs [see comments]
2. Familial occurrence of KID (keratitis, ichthyosis, deafness) syndrome
3. Keratitis, ichthyosis, and deafness (KID) syndrome. Vertical transmission and death from multiple squamous cell carcinomas
4. Hereditäre verhornungstörungen und taubheit.;Voigtländer V;Z Hautkr,1977
5. Female germline mosaicism in tuberous sclerosis confirmed by molecular genetic analysis
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1. Giant Juvenile Xanthogranuloma: Case Report, Literature Review, and Algorithm for Classification;Journal of Cutaneous Medicine and Surgery;2018-05-21
2. Oral squamous cell carcinoma in a patient with keratitis-ichthyosis-deafness syndrome: a rare case;Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology;2015-04
3. Keratitis, ichthyosis, and deafness (KID) syndrome: A review of infectious and neoplastic complications;Journal of the American Academy of Dermatology;2013-07
4. Disorders of Keratinization;Rook's Textbook of Dermatology;2010-05-06
5. Keratitis-Ichthyosis-Deafness Syndrome Caused by GJB2 Maternal Mosaicism;Journal of Investigative Dermatology;2009-03
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