Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
6 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
[Pallister-Killian syndrome in a Mexican mestizo patient. Case report].
Arch Argent Pediatr. 2018 Feb 1;116(1):e135-e138. doi: 10.5546/aap.2018.e135.
Arch Argent Pediatr. 2018.
PMID: 29333839
Free article.
Spanish.
[Genetic amniocentesis in high-risk populations. Experience in 3081 cases].
Cerrillo Hinojosa M, Yerena de Vega MC, González Panzzi ME, Godoy H, Galicia J, Gutiérrez Nájar A.
Cerrillo Hinojosa M, et al.
Ginecol Obstet Mex. 2009 Apr;77(4):173-82.
Ginecol Obstet Mex. 2009.
PMID: 19496509
Spanish.
Item in Clipboard
Antenatal Diagnosis of De Novo Balanced Structural Chromosome Aberrations in Latin America.
Méndez-Rosado LA, Quiñones-Masa O, Vaglio A, Quadrelli R, Sanchez-Peñarate D, Soriano-Torres M, Cerrillo-Hinojosa M, Escobedo-Aguirre F, Gutiérrez-Nájar A, Venegas-Barbosa P, Barrios-Martinez A, Echavarría-Estenoz D, Carbonell-de la Torre P, Pimentel-Benitez HI, González-Salé O, Hernádez-Gil J, de la Torre-Santos ME, Alonso-García Y, Cedeño-Aparicio N, Torriani-Mendoza P, Morales-Rodríguez E, Martín-García D, Cuétara-Lugo E, González-Domínguez N.
Méndez-Rosado LA, et al. Among authors: cerrillo hinojosa m.
MEDICC Rev. 2018 Oct;20(4):27-34. doi: 10.37757/MR2018.V20.N4.7.
MEDICC Rev. 2018.
PMID: 31242169
Free article.
Item in Clipboard
[Proposed normal values for alpha fetoprotein in maternal serum for the detection of neural tube closure defects and Down syndrome. Preliminary study].
Carreras de Paz JJ, Silva Mendoza JM, Violante Diaz M, Cerrillo Hinojosa M, Ahued Ahued JR.
Carreras de Paz JJ, et al. Among authors: cerrillo hinojosa m.
Ginecol Obstet Mex. 1991 Aug;59:261-4.
Ginecol Obstet Mex. 1991.
PMID: 1722478
Spanish.
Item in Clipboard
Uniparental disomy for chromosome 6 results in steroid 21-hydroxylase deficiency: evidence of different genetic mechanisms involved in the production of the disease.
López-Gutiérrez AU, Riba L, Ordoñez-Sánchez ML, Ramírez-Jiménez S, Cerrillo-Hinojosa M, Tusié-Luna MT.
López-Gutiérrez AU, et al. Among authors: cerrillo hinojosa m.
J Med Genet. 1998 Dec;35(12):1014-9. doi: 10.1136/jmg.35.12.1014.
J Med Genet. 1998.
PMID: 9863599
Free PMC article.
Item in Clipboard
Molecular genetic analysis of patients carrying steroid 21-hydroxylase deficiency in the Mexican population: identification of possible new mutations and high prevalence of apparent germ-line mutations.
Ordoñez-Sánchez ML, Ramírez-Jiménez S, López-Gutierrez AU, Riba L, Gamboa-Cardiel S, Cerrillo-Hinojosa M, Altamirano-Bustamante N, Calzada-León R, Robles-Valdés C, Mendoza-Morfin F, Tusié-Luna MT.
Ordoñez-Sánchez ML, et al. Among authors: cerrillo hinojosa m.
Hum Genet. 1998 Feb;102(2):170-7. doi: 10.1007/s004390050672.
Hum Genet. 1998.
PMID: 9580109
Item in Clipboard
Cite
Cite