Chromosome 11q13 deletion syndrome

Chromosome 11q13 deletion syndrome has been previously reported as either otodental syndrome or oculo-oto-dental syndrome. The otodental syndrome is characterized by dental abnormalities and high-frequency sensorineural hearing loss, and by ocular coloboma in some cases. The underlying genetic defec...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Yu-Seon, Kim, Gun-Ha, Byeon, Jung Hye, Eun, So-Hee, Eun, Baik-Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Pediatric Society 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5177688/
https://www.ncbi.nlm.nih.gov/pubmed/28018436
http://dx.doi.org/10.3345/kjp.2016.59.11.S10

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5177688/
https://www.ncbi.nlm.nih.gov/pubmed/28018436
http://dx.doi.org/10.3345/kjp.2016.59.11.S10

Ejemplares similares