Cargando…
Hay-Wells syndrome of ectodermal dysplasia: A rare autosomal dominant disorder
Autores principales: | Nagaveni, N. B., Umashankara, K. V. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3277001/ https://www.ncbi.nlm.nih.gov/pubmed/22346004 http://dx.doi.org/10.4103/0971-6866.92084 |
Ejemplares similares
-
Ectodermal Dysplasia Showing the Clinical Overlap between Hay Wells Syndrome and Bowen Armstrong Syndrome
por: Rachisan, Andreea Liana, et al.
Publicado: (2011) -
Autosomal Recessive Anhidrotic Ectodermal Dysplasia: A Rare Entity
por: Ghosh, Sangita, et al.
Publicado: (2014) -
EDAR mutation in autosomal dominant hypohidrotic ectodermal dysplasia in two Swedish families
por: Lind, Lisbet K, et al.
Publicado: (2006) -
Fetishistic transvestism with ectodermal dysplasia: A case report
por: Rohilla, Jitendra, et al.
Publicado: (2019) -
Mutations in GRHL2 Result in an Autosomal-Recessive Ectodermal Dysplasia Syndrome
por: Petrof, Gabriela, et al.
Publicado: (2014)