Síndrome de Williams: estudio clínico, citogenético, neurofisiológico y neuroanatómico
Background: Williams syndrome (WS) is a genetically based disorder caused by deletion of elastin and contiguous genes on chromosome 7q11.23. This syndrome is characterized by multiorganic involvement with dysmorphic facial features and a distinctive cognitive profile. It is an interesting model for...
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| Main Authors: | , , , , , , , , |
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| Language: | Spanish / Castilian |
| Published: |
Sociedad Médica de Santiago
2002
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| Subjects: | |
| Online Access: | http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872002000600005 |
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