Please use this identifier to cite or link to this item:
http://sgc.anlis.gob.ar/handle/123456789/601| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica | en_US |
| dc.date.accessioned | 2019-05-07T00:08:30Z | - |
| dc.date.available | 2019-05-07T00:08:30Z | - |
| dc.date.issued | 2016 | - |
| dc.identifier.uri | http://sgc.anlis.gob.ar/handle/123456789/601 | - |
| dc.description.abstract | El síndrome de Williams, síndrome de Williams-Beuren o también llamado monosomía 7 es un trastorno genético poco común, este es causado por una pérdida de material genético en el cromosoma 7. | en_US |
| dc.language.iso | es | en_US |
| dc.publisher | ANLIS Dr.C.G.Malbrán | en_US |
| dc.subject | Folleto Informativo para Pacientes | en_US |
| dc.subject | Síndrome de Williams | en_US |
| dc.subject | Trastornos de los Cromosomas | en_US |
| dc.subject | Anomalías Congénitas | en_US |
| dc.title | Síndrome de Williams-Beuren | en_US |
| dc.type | Póster | en_US |
| item.grantfulltext | open | - |
| item.openairetype | Póster | - |
| item.fulltext | With Fulltext | - |
| item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
| item.cerifentitytype | Publications | - |
| item.languageiso639-1 | es | - |
| Appears in Collections: | Folletos | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| FOLLETO_WBS.pdf | Folleto en español | 428.98 kB | Adobe PDF |  View/Open |
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