Syndromic and Non-Syndromic Primary Failure of Tooth Eruption: A Genetic Overview. [PDF]
Modafferi C +3 more
europepmc +1 more source
Transcriptome analysis identifies EDA1 variants disrupt FOSB-mediated regulation of odontogenic epithelial cell behaviors during dental germ development. [PDF]
Zhang J +6 more
europepmc +1 more source
Prenatal sonographic evidence of hypohidrotic ectodermal dysplasia and postnatal genetic testing of a family line of child. [PDF]
Lin D +9 more
europepmc +1 more source
Sparse Hair, Missing Teeth, Dry Skin: An Uncommon but Classic Condition.
Konda D, Reddy M.
europepmc +1 more source
A missense mutation in the highly conserved TNF-like domain of Ectodysplasin A is the candidate causative variant for X-linked hypohidrotic ectodermal dysplasia in Limousin cattle: Clinical, histological, and molecular analyses. [PDF]
Krull F, Bleyer M, Schäfer J, Brenig B.
europepmc +1 more source
Early recognition of hypohidrotic ectodermal dysplasia
Schneider Holm
doaj +1 more source
Treatment strategy for patient with non-syndromic tooth agenesis: a case report and literature review. [PDF]
Ouyang T +7 more
europepmc +1 more source
Hypohidrotic Ectodermal Dysplasia: Classical Clinical Features
Pratibha, Gupta +2 more
openaire +2 more sources
A Novel Ectodysplasin a Gene mutation of X-Linked Hypohidrotic Ectodermal Dysplasia. [PDF]
Zhuang Y +7 more
europepmc +1 more source

