Síndrome de Williams: estudio clínico, citogenético, neurofisiológico y neuroanatómico

Autor: Aravena C, Teresa, Castillo T, Silvia, Carrasco C, Ximena, Mena G, Ismael, López C, Javier, Rojas O, Juan P, Rosemberg P, Carol, Schröter G, Carolina, Aboitiz D, Francisco

Publikováno v: Revista médica de Chile v.130 n.6 2002
SciELO Chile
CONICYT Chile
instacron:CONICYT
Revista médica de Chile, Volume: 130, Issue: 6, Pages: 631-637, Published: JUN 2002

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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::ca0bab610c475d9342504acfdf978dd5
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872002000600005