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The novel polymorphic variants within the paired box of the PAX9 gene are associated with selective tooth agenesisRecent advances in understanding of the molecular basis of anhidrotic ectodermal dysplasia: discovery of a ligand, ectodysplasin A and its two receptors.A novel mutation in the ED1 gene in a patient with X-linked hypohidrotic ectodermal dysplasia.Sequence polymorphisms of the EDA and the DL genes in the patients with an X-linked and an autosomal forms of anhidrotic ectodermal dysplasiaNovel mutation in the 5' splice site of exon 4 of the TCOF1 gene in the patient with Treacher Collins syndrome[Paternity exclusion tests in the Department of Forensic Medicine, University of Medical Sciences in Poznan]A rare heterozygous TRAF6 variant is associated with hypohidrotic ectodermal dysplasiaA new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia
P50
Q28190561-7CB496B6-CD4F-45A7-AD34-E3CDAFC0BFABQ34708164-BC5D5ACC-4628-458F-9E2A-F167C0AE424AQ44580204-4C5FB1B6-F2AC-4FFE-811C-9AFEBD899ED4Q73931370-6A9F54B2-5EBC-4765-AE09-8972B30871C4Q79249807-FEE1328A-43FC-44BA-8DD9-06F7DE686AEFQ79648632-2E43AFCB-C418-4DE1-884F-C13A0FED8F89Q83378953-F3C0F353-5D68-4002-A104-0ED2BFEC0B63Q84787906-83BDD417-3D50-4CDA-8CCD-9FF8896AD273
P50
description
researcher
@en
wetenschapper
@nl
name
A S Wiśniewski
@en
A S Wiśniewski
@nl
type
label
A S Wiśniewski
@en
A S Wiśniewski
@nl
prefLabel
A S Wiśniewski
@en
A S Wiśniewski
@nl
P106
P31
P496
0000-0003-4935-0733