Zobrazeno 1 - 8
of 8
pro vyhledávání: '"María Solo de Zaldívar"'
Autor:
Elena María Márquez Isidro, María Jesús García García, María Solo de Zaldívar Tristancho, Rafael Romero Peguero
Publikováno v:
Anales de Pediatría, Vol 95, Iss 5, Pp 375-377 (2021)
Externí odkaz:
https://doaj.org/article/3230b2e16c284d789f9097c88bb61969
Autor:
Elena María Márquez Isidro, María Jesús García García, María Solo de Zaldívar Tristancho, Rafael Romero Peguero
Publikováno v:
Anales de Pediatría (English Edition), Vol 95, Iss 5, Pp 375-377 (2021)
Externí odkaz:
https://doaj.org/article/97a6f1fa3a0a400eb0b8a11b8e0c8887
Autor:
María Jesús García García, Rafael Romero Peguero, María Solo de Zaldívar Tristancho, Elena María Márquez Isidro
Publikováno v:
Anales de Pediatría (English Edition), Vol 95, Iss 5, Pp 375-377 (2021)
Anales De Pediatria
Anales De Pediatria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::757c43a04cf6ea6190a6e0ae6a60f135
https://doi.org/10.1016/j.anpede.2021.05.005
https://doi.org/10.1016/j.anpede.2021.05.005
Autor:
Ignacio Arroyo Carrera, María Solo de Zaldívar Tristancho, Verónica Deyanira García-Navas Núñez, Alba Ramajo Polo, Marta Gutiérrez Agujetas
Publikováno v:
Revista de Neurología. 76:111
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17b2b18e549f2df15cd2c95e08d1d530
https://doi.org/10.33588/rn.7603.2022165
https://doi.org/10.33588/rn.7603.2022165
Akademický článek
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Autor:
Thomas Eggermann, María Solo de Zaldívar, Matthias Begemann, Lukas Soellner, Ignacio Arroyo Carrera, Rebeca Martín
Publikováno v:
American journal of medical genetics. Part A. 170(3)
The association of maternal uniparental disomy of human chromosome 7 (upd(7) mat) and the growth retardation disorder Silver-Russell syndrome (SRS) is well established, but the causative gene or region is currently unknown. However, several observati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::380ebdc475ce0b50c1d5cafe348e5b6c
https://pubmed.ncbi.nlm.nih.gov/26663145
https://pubmed.ncbi.nlm.nih.gov/26663145
Autor:
Alexandra MacDonald, Amparo López-Lafuente, María Solo de Zaldívar Tristancho, José Luis Gómez-Skarmeta, Eva Bermejo-Sánchez, Ángel Zúñiga, María Luisa Martínez-Frías, María Luisa Martínez-Fernández, Ignacio Arroyo-Carrera
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
Warburg-Micro syndrome (WARBM) is an autosomal recessive syndrome characterized by microcephaly, microphthalmia, microcornea, congenital cataracts, optic atrophy and central nervous system malformations. This syndrome is caused by mutations in the RA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc0f565428b8df3d9bd606d90083064d
http://hdl.handle.net/10261/129541
http://hdl.handle.net/10261/129541
Autor:
Francisco Jimenez Parrilla, Antonio Perez Sanchez, Antonio Losada Martinez, María Solo de Zaldívar Tristancho, Eva Ximénez Verresen, José Fernando Ferreira Pérez
Publikováno v:
Early Human Development. 84:S17-S18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0f0ca8854d612399303f3889d7ddf29
https://doi.org/10.1016/j.earlhumdev.2008.09.043
https://doi.org/10.1016/j.earlhumdev.2008.09.043