Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Alejandra Moreno‐Chacón"'
Autor:
Verónica Fabiola Morán‐Barroso, Alicia Cervantes, María del Refugio Rivera‐Vega, Adriana del Castillo‐Moreno, Alejandra Moreno‐Chacón, Estefanía Mejía‐Cauich, Laura Eréndira Contreras‐Ortiz, Fernando Fernández‐Ramírez
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 9, Pp n/a-n/a (2021)
Abstract Background Trisomy 13 or Patau syndrome has a prevalence of 1:10,000–20,000 and is characterized by microcephaly, microphthalmia, polydactyly, as well as other dysmorphic features and malformations, with a patient survival of 13% in the fi
Externí odkaz:
https://doaj.org/article/7fb0fbec534a46f6a92679c82a5aa3e2
Autor:
Verónica Fabiola Morán-Barroso, Fernando Fernández-Ramírez, Laura Eréndira Contreras-Ortiz, Adriana Del Castillo-Moreno, Estefanía Mejía-Cauich, M.R. Rivera-Vega, Alejandra Moreno-Chacón, Alicia Cervantes
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 9, Iss 9, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine, Vol 9, Iss 9, Pp n/a-n/a (2021)
Background Trisomy 13 or Patau syndrome has a prevalence of 1:10,000–20,000 and is characterized by microcephaly, microphthalmia, polydactyly, as well as other dysmorphic features and malformations, with a patient survival of 13% in the first year.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a469fdd2587bb29481361797dc7c1394
https://pubmed.ncbi.nlm.nih.gov/34288579
https://pubmed.ncbi.nlm.nih.gov/34288579