Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Idalid Cuero-Quezada"'
Autor:
Gerardo E. Fabián-Morales, Lucina Bobadilla-Morales, Christian Peña-Padilla, Rafael Nieto-García, Pascuala B. Rivera-Ramírez, Alfredo Corona-Rivera, Aurea Márquez-Mora, Graciela Macías-Salcedo, Idalid Cuero-Quezada, Jorge R. Corona-Rivera
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 79, Iss 6 (2022)
Background: Congenital heart defects (CHD) are among the most frequent manifestations of 22q11.2 deletion syndrome. Although we found relatively few studies aimed at specifically detecting 22q11.2 deletion in newborns (NB) with CHD, none of them has
Externí odkaz:
https://doaj.org/article/dfc31b69b4044c08b4a126ab9777b5ef
Autor:
Christian Peña-Padilla, Jorge Román Corona-Rivera, Idalid Cuero-Quezada, Yaneris M. Romero-Bolaño, Jennifer Santana-Hernández, Alfredo Corona-Rivera, Alejandra Baldomero-López, Lucina Bobadilla-Morales, Cristian Irela Aranda-Sánchez
Publikováno v:
Congenital Anomalies. 61:188-192
Our study investigated the role of MTHFR C677T and A1298C variants in infants with neural tube defects (NTDs) from western Mexico. Using TaqMan allelic discrimination assay, we genotyped 101 live-born patients with NTDs (cases) and 247 controls. Our
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48fc4751e1d40946d7f4c1a2feb1c12c
https://doi.org/10.1111/cga.12429
https://doi.org/10.1111/cga.12429
Autor:
María Teresa Alejandra González-Rodríguez, Sinhue Alejandro Brukman-Jiménez, Idalid Cuero-Quezada, Jorge Román Corona-Rivera, Alfredo Corona-Rivera, Graciela Serafín-Saucedo, Liuba M. Aguirre-Salas, Lucina Bobadilla-Morales
Publikováno v:
Genes. 14:253
Turner Syndrome is characterized by a normal X chromosome and the partial or complete absence of a second sexual chromosome. Small supernumerary marker chromosomes are present in 6.6% of these patients. Because of the wide range of Turner syndrome ka
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37dedfcbdb45f4d4c61e20ba090aaff8
https://doi.org/10.3390/genes14020253
https://doi.org/10.3390/genes14020253