18p-syndrome: Presentation of two cases with alobar holoprosencenphaly
Introduction: The syndrome by deletion of the short arm of chromosome 18 is an infrequent syndrome, and its phenotypical variability makes it difficult to recognize. Its most frequently observed clinical characteristics include mental retardation, growth retardation, craniofacial malformations, incl...
- Autores:
-
Pachajoa Londoño, Harry Mauricio
Isaza, Carolina
Saldarriaga, Wilmar
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2010
- Institución:
- Universidad ICESI
- Repositorio:
- Repositorio ICESI
- Idioma:
- spa
- OAI Identifier:
- oai:repository.icesi.edu.co:10906/78341
- Acceso en línea:
- http://www.scopus.com/inward/record.url?eid=2-s2.0-78650737753&partnerID=tZOtx3y1
http://hdl.handle.net/10906/78341
- Palabra clave:
- Ciencias socio biomédicas
Biomedical sciences
Síndrome
Cromosoma 18
Genes
- Rights
- openAccess
- License
- https://creativecommons.org/licenses/by-nc-nd/4.0/