Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Miguel Ángel Alcántara Ortigoza"'
Autor:
Mara Medeiros, Sandra Enciso, Ana María Hernández, Hector Rodrigo García Hernández, Georgina Toussaint, Claudia Pinto, Elsy Maureen Navarrete Rodríguez, Blanca E. del-Rio-Navarro, Omar Josué Saucedo-Ramírez, Patricia Medina Bravo, Sergio Miranda, Liliana Worona, Germán Sosa, Leticia Belmont Martinez, Miguel Ángel Alcántara Ortigoza, Laura Escobar, Ricardo Muñoz Arizpe
Publikováno v:
Nefrología (English Edition), Vol 36, Iss 3, Pp 323-325 (2016)
Externí odkaz:
https://doaj.org/article/a8248b3ad1bf4b919b0ff48378f3efbd
Autor:
Mara Medeiros, Sandra Enciso, Ana María Hernández, Hector Rodrigo García Hernández, Georgina Toussaint, Claudia Pinto, Elsy Maureen Navarrete Rodríguez, Blanca E. del-Rio-Navarro, Omar Josué Saucedo-Ramírez, Patricia Medina Bravo, Sergio Miranda, Liliana Worona, Germán Sosa, Leticia Belmont Martinez, Miguel Ángel Alcántara Ortigoza, Laura Escobar, Ricardo Muñoz Arizpe
Publikováno v:
Nefrología, Vol 36, Iss 3, Pp 323-325 (2016)
Externí odkaz:
https://doaj.org/article/4f590a0a8eb140e383a793e4d834c193
Autor:
Miguel Ángel Alcántara Ortigoza, Daniel Martínez Anaya, Liliana Fernández Hernández, Verónica Ulloa Avilés, Ariadna González-del Angel, Patricia Pérez Vera
Publikováno v:
Cytogenetic and genome research. 160(4)
Nonmosaic trisomy involving 19p13.3p13.2 is a very uncommon abnormality. At present, only 12 cases with this genetic condition have been reported in the literature. However, the size of the trisomic fragment is heterogeneous and thus, the clinical sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ad64cb3c30477b0744297714fd4c9ba
https://pubmed.ncbi.nlm.nih.gov/32369810
https://pubmed.ncbi.nlm.nih.gov/32369810
Autor:
Blanca E. Del-Rio-Navarro, Ana Hernandez, Liliana Worona, Patricia Medina Bravo, Georgina Toussaint, Claudia Pinto, Germán Sosa, Elsy Maureen Navarrete Rodríguez, Miguel Ángel Alcántara Ortigoza, Ricardo Muñoz Arizpe, Sergio Miranda, Hector Rodrigo García Hernández, Laura I. Escobar, Mara Medeiros, Omar Josué Saucedo-Ramírez, Leticia Belmont Martinez, Sandra Enciso
Publikováno v:
Nefrología (English Edition), Vol 36, Iss 3, Pp 323-325 (2016)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e7c9b2a5e33bf2bd7c38e492b67090c
http://www.sciencedirect.com/science/article/pii/S2013251416300190
http://www.sciencedirect.com/science/article/pii/S2013251416300190
Publikováno v:
Acta Pediátrica de México, Vol 33, Iss 6, Pp 324-328 (2014)
Phenylketonuria (PKU) is an autosomic recessive inborn errors of metabolism. It is caused y the deficiency of phenylalanine hydroxylase, an enzyme encoded by the PAH gene in 12q22. This gene has a wide mutation spectrum and several different genotype
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::57fa078ed0415be31cb53fc2d019e755
http://ojs.actapediatrica.org.mx/index.php/APM/article/view/595
http://ojs.actapediatrica.org.mx/index.php/APM/article/view/595
Autor:
Miguel Ángel Alcántara-Ortigoza, Leticia Belmont-Martínez, Marcela Vela-Amieva, Ariadna González-Del Angel
Publikováno v:
Genetic Testing; Sep2008, Vol. 12 Issue 3, p409-414, 6p