Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Aurea Márquez-Mora"'
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:
Mireya Orozco-Vela, Jorge Román Corona-Rivera, Christian Peña-Padilla, Aurea Márquez-Mora, Rosa Margarita Cruz-Osorio, Alejandra Baldomero-López, Alfredo Corona-Rivera, Lucero Mendoza-Maldonado, Lucina Bobadilla-Morales, César Cenobio Barba-Barba
Publikováno v:
American Journal of Medical Genetics Part A. 182:2085-2093
Transient abnormal myelopoiesis (TAM) raises the risk for acute myeloid leukemia of Down syndrome (DS) (ML-DS), and both are related to GATA1 pathogenic variants. Here, we analyzed which findings on complete blood count (CBC) are associated with TAM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4512285ce4ad053e38a49e5dafde8f60
https://doi.org/10.1002/ajmg.a.61748
https://doi.org/10.1002/ajmg.a.61748