C. García-Delgado

发表

Caudal duplication with multicystic dysplastic kidney: a case report.

C. García-Delgado, Paola Mendelsberg-Fishbein, Fernando González-Ledón, 2015, Clinical dysmorphology.

Out-of-pocket expenditures and care time for children with Down Syndrome: A single-hospital study in Mexico City

G. Salinas-Escudero, María Teresa Tiro-Sánchez, Filiberto Toledano-Toledano, 2019, PloS one.

Importancia del diagnóstico de mutaciones en el gen de la conexina 26 en el manejo integral de la sordera congénita no sindrómica Importance of the diagnosis of connexin 26 gene mutations in the integral management of non-syndromic congenital deafness

J. Aguirre-Hernández, B. A. Rodríguez-Espino, E. R. Vázquez-Martínez, 2013 .

Importance of the diagnosis of protein connexin 26 mutations in the integral management of nonsyndromic congenital deafness

A. Act, J. Aguirre-Hernández, B. A. Rodríguez-Espino, 2013 .

Nance–Horan syndrome in females due to a balanced X;1 translocation that disrupts the NHS gene: Familial case report and review of the literature

J. Villa-Morales, Karem Nieto-Martínez, A. Martínez-Herrera, 2018, Ophthalmic genetics.

A familial reciprocal translocation t(1;15) in three generations identified in a regular trisomy 21 patient.

J. Villa-Morales, A. Luna-Angulo, C. García-Delgado, 2010, Genetic counseling.

Mutational spectrum of EDA and EDAR genes in a cohort of Mexican mestizo patients with hypohidrotic ectodermal dysplasia

M. Toledo-Bahena, M. López-López, M. Cerbón, 2017, Journal of the European Academy of Dermatology and Venereology : JEADV.

Clinical profile of a patient cohort with Beckwith-Wiedemann syndrome treated at the Hospital Infantil de México Federico Gómez (2007 to 2012)

A. Act, Rosenda I. Peñaloza-Espinosa, C. García-Delgado, 2013 .

Cytogenetic profile in 1,921 cases of trisomy 21 syndrome.

A. Cervantes, C. García-Delgado, V. Morán-Barroso, 2015, Archives of medical research.

[Clinical profile of a cohort of Silver-Russell syndrome patients followed at the Hospital Infantil de México Federico Gómez from 1998 to 2012].

C. García-Delgado, V. Morán-Barroso, L. García-Morales, 2014, Boletin medico del Hospital Infantil de Mexico.

Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes

J. Villa-Morales, J. Berumen, Karem Nieto-Martínez, 2014, BMC Medical Genomics.

Congenital hearing loss: a literature review of the genetic etiology in a Mexican population.

D. Villanueva-García, C. García-Delgado, V. Morán-Barroso, 2022, Boletin medico del Hospital Infantil de Mexico.

Congenital macroglossia: clinical features and therapeutic strategies in pediatric patients

L. Jasso-Gutiérrez, C. García-Delgado, V. Morán-Barroso, 2016 .

Clinical, Cytogenetic, and Biochemical Analyses of a Family with a t(3;13)(q26.2;p11.2): Further Delineation of 3q Duplication Syndrome

A. Luna-Angulo, A. Cervantes, M. Abreu-González, 2013, Case reports in genetics.

Niemann-Pick disease A or B in four pediatric patients and SMPD1 mutation carrier frequency in the Mexican population.

P. Valencia-Mayoral, M. Cerbón, A. Ortega-Vázquez, 2019, Annals of hepatology.

Polymorphism analysis and new JAG1 gene mutations of Alagille syndrome in Mexican population

P. Valencia-Mayoral, M. Cerbón, J. Zenteno, 2013, Meta gene.

Velocardiofacial syndrome in Mexican patients: Unusually high prevalence of congenital heart disease.

P. Medina-Bravo, N. Garibay-Nieto, R. Sánchez-Urbina, 2015, International journal of pediatric otorhinolaryngology.

Brachmann-Cornelia de Lange syndrome with a papilloma of the choroid plexus: analyses of molecular genetic characteristics of the patient and the tumor. A single-case study

F. Arenas-Huertero, M. Pérezpeña-Díazconti, E. Castro-Sierra, 2014, Child's Nervous System.

Monosomy 9p24 in two non-related patients as result of a translocation (2;9).

A. Cervantes, C. Serrano-Bello, C. García-Delgado, 2018, Archivos Argentinos de Pediatria.

No evidence of linkage for cleft lip with or without cleft palate to a marker near the transforming growth factor alpha locus in two populations.

T. Beaty, D. Wyszynski, N. Maestri, 1997, Human heredity.

Evidence for an association between markers on chromosome 19q and non-syndromic cleft lip with or without cleft palate in two groups of multiplex families

T. Beaty, D. Wyszynski, N. Maestri, 1996, Human Genetics.

Craniosynostosis, delayed closure of the fontanelle, anal, genitourinary, and skin abnormalities (CDAGS syndrome): first report in a Mexican patient and review of the literature

M. Toledo-Bahena, C. Mena-Cedillos, A. Valencia-Herrera, 2017, International journal of dermatology.

A Novel c.91dupG JAG1 Gene Mutation Is Associated with Early Onset and Severe Alagille Syndrome

P. Valencia-Mayoral, M. Cerbón, E. R. Vázquez-Martínez, 2018, Case reports in genetics.

Escobar syndrome with heterotaxia and esophageal atresia: case report.

M. Pérezpeña-Díazconti, C. García-Delgado, V. Morán-Barroso, 2014, Genetic counseling.

[Clinical profile of a cohort of Silver-Russell syndrome patients followed at the Hospital Infantil de México Federico Gómez from 1998 to 2012].

C. García-Delgado, V. Morán-Barroso, L. García-Morales, 2014, Boletin medico del Hospital Infantil de Mexico.

Clinical profile of a cohort of Silver-Russell syndrome patients followed at the Hospital Infantil de México Federico Gómez from 1998 to 2012

C. García-Delgado, V. Morán-Barroso, L. García-Morales, 2020 .

Síndrome de Beckwith-Wiedemann Beckwith-Wiedemann syndrome

M. Pérezpeña-Díazconti, Eduardo, C. García-Delgado, 2009 .

Congenital hypertrichosis universalis in Mexican female twins

A. Valencia-Herrera, A. Cervantes, S. Kofman, 2016, International journal of dermatology.