Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Jennifer Santana-Hernández"'
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:
Izabel Maryalexandra, Rios-Flores, Lucina, Bobadilla-Morales, Christian, Peña Padilla, Alfredo, Corona-Rivera, Elizabeth, Acosta-Fernández, Jennifer, Santana-Hernández, Sinhue Alejandro, Brukman-Jiménez, Jorge Román, Corona Rivera
Publikováno v:
Revista medica del Instituto Mexicano del Seguro Social. 59(2)
Prader Willi syndrome (PWS) and Angelman syndrome (AS) are neurodevelopmental disorders caused by deletions or methylation defects, making a loss of expression of imprinted genes located in the 15q11-q13 region, and these can be assessed by different
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6f35fe02bfb242f411305ae0d9c12c21
https://pubmed.ncbi.nlm.nih.gov/34232598
https://pubmed.ncbi.nlm.nih.gov/34232598