C Garcia Delgado
Overview
Explore the profile of C Garcia Delgado including associated specialties, affiliations and a list of published articles.
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Articles
7
Citations
201
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0
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Recent Articles
1.
Navarrete-Rodriguez E, Del-Rio-Navarro B, Garcia-Fajardo D, Baay-Guzman G, Espinosa-Padilla S, Medina-Torres E, et al.
Allergol Immunopathol (Madr)
. 2018 Oct;
47(2):141-151.
PMID: 30292446
Background: The del22q11 syndrome patients present immunological abnormalities associated to thymus alterations. Up to 75% of them present cardiopathies and thymus is frequently removed during surgery. The thymectomy per se...
2.
Flores Ramirez F, Abreu Gonzalez M, Delgado C, Aparicio Onofre A, Guevara Yanez R, Sanchez Urbina R, et al.
Genet Couns
. 2011 Feb;
21(4):363-73.
PMID: 21290965
We describe a patient who had multiple malformations including ventriculomegaly, colpocephaly, corpus callosum, cerebellum and vermix hypoplasia, optic nerve hypoplasia, corneal opacity and congenital heart disease in whom a trisomy...
3.
Cano Portero R, Delgado C, de Mateo Ontanon S
Rev Esp Salud Publica
. 2000 Oct;
74(4):369-75.
PMID: 11031845
Background: The change in the epidemiological pattern undergone by meningococcal disease in a large part of the country in the 1996-1997 season and the decision to intervene by means of...
4.
Howard T, Paznekas W, Green E, Chiang L, Ma N, Ortiz de Luna R, et al.
Nat Genet
. 1997 Jan;
15(1):36-41.
PMID: 8988166
Saethre-Chotzen syndrome is one of the most common autosomal dominant disorders of craniosynostosis in humans and is characterized by craniofacial and limb anomalies. The locus for Saethre-Chotzen syndrome maps to...
5.
6.
Gonzalez-Ramos M, Eguiarte Ortega M, Costa Miro M, GONZALEZ RIVERA E, Delgado C
Bol Med Hosp Infant Mex
. 1976 Nov;
33(6):1423-33.
PMID: 1008935
We are presenting five cases of Goldenhar's syndrome studied at the Clinical Genetics Unit of the Hospital Infantil of México. We do not know exactly the type of inheritance of...
7.
Gonzalez-Ramos M, De Valencia E, Delgado C, Macias M
Bol Med Hosp Infant Mex
. 1976 Mar;
33(2):403-10.
PMID: 177027
We present six cases of ADAM syndrome, that we have been studying at the Unit of Clinical Genetics of the Hospital Infantil de México. We wish to stress how it...