QuickView for ectodermal dysplasia (phenotype)

1. Skin from GRHL2 mutant patients with ectodermal dysplasia and hearing loss
2. Neonatal keratinocytes with ΔNp63α overexpression or p63 siRNA knockdown
3. Mouse Phenotypes - Ectodermal dysplasia
4. OMIM - Congenital disorder
5. Skin fibroblasts derived from Setleis Syndrome patients (Twist2 null) and normal controls

1. Nectinopathies: an emerging group of ectodermal dysplasia syndromes.
2. Ectodermal dysplasias: the p63 tail.
3. Infantile bilateral glaucoma in a child with ectodermal dysplasia.
4. Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal…
5. Diagnosis and treatment in anhidrotic ectodermal dysplasia with immunodeficiency.

Task java.util.concurrent.FutureTask@81ffe76 rejected from java.util.concurrent.ThreadPoolExecutor@5688fd26[Running, pool size = 100, active threads = 99, queued tasks = 0, completed tasks = 20495651]