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...
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| Publicat a: | Colombia Médica |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Espanhol |
| Publicat: |
Universidad del Valle
2010
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| Matèries: | |
| Accés en línia: | https://www.redalyc.org/articulo.oa?id=28315594011 |
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