Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

62 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
[ADAM syndrome].
González-Ramos M, de Valencia EL, García Delgado C, Macías MA. González-Ramos M, et al. Among authors: garcia delgado c. Bol Med Hosp Infant Mex. 1976 Mar-Apr;33(2):403-10. Bol Med Hosp Infant Mex. 1976. PMID: 177027 Spanish.
Clinical delineation of a patient with trisomy 1q32.qter and monosomy 5p resulting from a familial translocation 1;5.
Flores Ramírez F, Abreu González M, García Delgado C, Aparicio Onofre A, Guevara Yáñez R, Sánchez Urbina R, Murguía Peniche T, Ramírez-Ortíz MA, Ibarra Ríos D, Ortiz de Luna RI, Cervantes Peredo AB, Morán Barroso VF. Flores Ramírez F, et al. Among authors: garcia delgado c. Genet Couns. 2010;21(4):363-73. Genet Couns. 2010. PMID: 21290965
[Goldenhar's syndrome].
González-Ramos M, Eguiarte Ortega MC, Costa Miró M, González Rivera EL, García Delgado C. González-Ramos M, et al. Among authors: garcia delgado c. Bol Med Hosp Infant Mex. 1976 Nov-Dec;33(6):1423-33. Bol Med Hosp Infant Mex. 1976. PMID: 1008935 Spanish.
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.
Gómez-Laguna L, Martínez-Herrera A, Reyes-de la Rosa ADP, García-Delgado C, Nieto-Martínez K, Fernández-Ramírez F, Valderrama-Atayupanqui TY, Morales-Jiménez AB, Villa-Morales J, Kofman S, Cervantes A, Morán-Barroso VF. Gómez-Laguna L, et al. Among authors: garcia delgado c. Ophthalmic Genet. 2018 Jan-Feb;39(1):56-62. doi: 10.1080/13816810.2017.1363245. Epub 2017 Sep 18. Ophthalmic Genet. 2018. PMID: 28922055 Review.
[Monosomy 9p24 in two non-related patients as result of a translocation (2;9)].
León-Carlos NY, García-Delgado C, Morales-Jiménez AB, Serrano-Bello C, Cervantes A, Morán Barroso VF. León-Carlos NY, et al. Among authors: garcia delgado c. Arch Argent Pediatr. 2018 Aug 1;116(4):e603-e608. doi: 10.5546/aap.2018.e603. Arch Argent Pediatr. 2018. PMID: 30016040 Free article. Spanish.
Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes.
Cervantes A, García-Delgado C, Fernández-Ramírez F, Galaz-Montoya C, Morales-Jiménez AB, Nieto-Martínez K, Gómez-Laguna L, Villa-Morales J, Quintana-Palma M, Berúmen J, Kofman S, Morán-Barroso VF. Cervantes A, et al. Among authors: garcia delgado c. BMC Med Genomics. 2014 Sep 15;7:55. doi: 10.1186/1755-8794-7-55. BMC Med Genomics. 2014. PMID: 25223409 Free PMC article.
Clinical, Cytogenetic, and Biochemical Analyses of a Family with a t(3;13)(q26.2;p11.2): Further Delineation of 3q Duplication Syndrome.
Abreu-González M, García-Delgado C, Cervantes A, Aparicio-Onofre A, Guevara-Yáñez R, Sánchez-Urbina R, Gallegos-Arreola MP, Luna-Angulo A, Estrada FJ, Morán-Barroso VF. Abreu-González M, et al. Among authors: garcia delgado c. Case Rep Genet. 2013;2013:895259. doi: 10.1155/2013/895259. Epub 2013 Sep 18. Case Rep Genet. 2013. PMID: 24151567 Free PMC article.
Cytogenetic profile in 1,921 cases of trisomy 21 syndrome.
Flores-Ramírez F, Palacios-Guerrero C, García-Delgado C, Morales-Jiménez AB, Arias-Villegas CM, Cervantes A, Morán-Barroso VF. Flores-Ramírez F, et al. Among authors: garcia delgado c. Arch Med Res. 2015 Aug;46(6):484-9. doi: 10.1016/j.arcmed.2015.08.001. Epub 2015 Aug 24. Arch Med Res. 2015. PMID: 26314225
62 results