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Publikováno v:
Journal of dentistry for children (Chicago, Ill.). 86(1)
Pachyonychia congenita (PC) is a rare autosomal dominant condition caused by heterozygous mutation in one of five keratin genes. The purpose of this paper is to report a five-day-old infant with PC whose initial presentation revealed multiple malform
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d451cfb9e23de887039dd3d1e5735281
https://pubmed.ncbi.nlm.nih.gov/30992103
https://pubmed.ncbi.nlm.nih.gov/30992103
