Epiloia: estudio multidisciplinario de un caso
Epiloia it's a genetic disease with dominant autosomic source which presents alterations in chromosomes 9 and 16. The clinical picture is typical and laboratory findings permit to make a precise diagnosis. In the study a 27 year old with this disorder was examined, he presented epileptic seizur...
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Main Authors: | , , |
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Formato: | Libro |
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Universidad de Antioquia,
2004-01-01T00:00:00Z.
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Acceso en liña: | Connect to this object online. |
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Internet
Connect to this object online.3rd Floor Main Library
Número de Clasificación: |
A1234.567 |
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Copia 1 | Dispoñible |