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pro vyhledávání: '"Villota Delgado, Vania Alexandra"'
Publikováno v:
Repositorio ICESI
Universidad ICESI
instacron:Universidad ICESI
Universidad ICESI
instacron:Universidad ICESI
Mowat-Wilson syndrome (MWS) is a very infrequent congenital polimalformative disorder, caused by mutations, deletions or insertions of the ZEB2 gene, which codify for a protein that is involved in the migration of the neural crest cells and the devel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::5b239249e89640f0888aa8907d19b2f9
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0370-41062012000400008&lng=en&nrm=iso&tlng=en
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0370-41062012000400008&lng=en&nrm=iso&tlng=en
Autor:
Pachajoa, Harry, Ruiz-Botero, Felipe, Meza-Escobar, Luis Enrique, Villota-Delgado, Vania Alexandra, Ballesteros, Adriana, Padilla, Ivan, Duarte, Diana
Publikováno v:
Journal of Medical Case Reports; 9/26/2016, Vol. 10, p1-6, 6p
