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Boletin Medico Del Hospital Infantil De Mexico|February 9, 2018
[Congenital macroglossia: clinical features and therapeutic strategies in paediatric patients]Paulina María Núñez-Martínez, Constanza García-Delgado, Verónica Fabiola Morán-Barroso, et al.
Boletin Medico Del Hospital Infantil De Mexico|February 9, 2018
[Clinical profile of a cohort of Silver-Russell syndrome patients followed at the Hospital Infantil de México Federico Gómez from 1998 to 2012]Carolina Isabel Galaz-Montoya, Constanza García-Delgado, Alicia Cervantes-Peredo, et al.
Archivos Argentinos De Pediatria|July 18, 2018
Monosomy 9p24 in two non-related patients as result of a translocation (2;9)Nayla Y León-Carlos, Constanza García-Delgado, Ariadna B Morales-Jiménez, et al.
Archives of Medical Research|August 29, 2015
Cytogenetic profile in 1,921 cases of trisomy 21 syndromeFrancisco Flores-Ramírez, Claudia Palacios-Guerrero, Constanza García-Delgado, et al.
Case Reports in Genetics|July 27, 2018
A Novel c.91dupG JAG1 Gene Mutation Is Associated with Early Onset and Severe Alagille SyndromeAlejandra Del Pilar Reyes-de la Rosa, Gustavo Varela-Fascinetto, Constanza García-Delgado, et al.
Archivos Argentinos De Pediatria|January 16, 2018
[Pallister-Killian syndrome in a Mexican mestizo patient. Case report]Paola Mendelsberg-Fishbein, Constanza García-Delgado, Linda B Muñoz-Martínez, et al.
Plos One|January 11, 2019
Out-of-pocket expenditures and care time for children with Down Syndrome: A single-hospital study in Mexico CitySilvia Martínez-Valverde, Guillermo Salinas-Escudero, Constanza García-Delgado, et al.
Boletin Medico Del Hospital Infantil De Mexico|July 28, 2020
X-linked hypohidrotic ectodermal dysplasia by a de novo recurrent variant in a Mexican patientMiguel A Noriega-Juárez, Constanza García-Delgado, América Villaseñor-Domínguez, et al.
International Journal of Dermatology|February 21, 2017
Craniosynostosis, delayed closure of the fontanelle, anal, genitourinary, and skin abnormalities (CDAGS syndrome): first report in a Mexican patient and review of the literatureRodrigo Pastrana-Ayala, Gretty L Peña-Castro, Adriana M Valencia-Herrera, et al.
BMC Medical Genomics|September 17, 2014
Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromesAlicia Cervantes, Constanza García-Delgado, Fernando Fernández-Ramírez, et al.
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