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Glover, Guillermo
338
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Online (337)
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Articles (Online) (44)
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1
Geographic distribution and phenotype of European people wi..:
Mondejar-Lopez, Pedro
;
Zolin, Anna
;
Garcia-Marcos, Patricia W.
...
Respiratory Medicine. 192 (2022) - p. 106736 , 2022
Link:
https://doi.org/10.1016/..
?
2
Molecular Testing for Fragile X: Analysis of 5062 Tests fro..:
Tejada, María-Isabel
;
Glover, Guillermo
;
Martínez, Francisco
...
BioMed Research International. 2014 (2014) - p. 1-8 , 2014
Link:
https://doi.org/10.1155/..
?
3
Molecular characterization of a new patient with a non‐recu..:
Vera‐Carbonell, Ascensión
;
López‐Expósito, Isabel
;
Bafalliu, Juan Antonio
...
American Journal of Medical Genetics Part A. 152A (2010) 10 - p. 2670-2680 , 2010
Link:
https://doi.org/10.1002/..
?
4
CFTR H609R mutation in Ecuadorian patients with cystic fibr..:
Moya-Quiles, María Rosa
;
Glover, Guillermo
;
Mondéjar-López, Pedro
...
Journal of Cystic Fibrosis. 8 (2009) 4 - p. 280-281 , 2009
Link:
https://doi.org/10.1016/..
?
5
New strategy for the prenatal detection/exclusion of patern..:
Bustamante-Aragones, Ana
;
Gallego-Merlo, Jesus
;
Trujillo-Tiebas, Maria Jose
...
Journal of Cystic Fibrosis. 7 (2008) 6 - p. 505-510 , 2008
Link:
https://doi.org/10.1016/..
?
6
Fragile X screening program in a spanish region:
Gabarrón, Joaquina
;
Lopez, Isabel
;
Glover, Guillermo
.
American Journal of Medical Genetics. 43 (1992) 1-2 - p. 333-338 , 1992
Link:
https://doi.org/10.1002/..
?
7
Molecular testing for fragile X: analysis of 5062 tests fro..:
Tejada, María-Isabel
;
Glover, Guillermo
;
Martínez, Francisco
...
http://www.hindawi.com/journals/bmri/2014/195793/abs/. , 2014
Link:
http://hdl.handle.net/10..
?
8
Molecular testing for fragile X: analysis of 5062 tests fro..:
Tejada, María-Isabel
;
Glover, Guillermo
;
Martínez, Francisco
...
http://www.hindawi.com/journals/bmri/2014/195793/abs/. , 2014
Link:
http://hdl.handle.net/10..
?
9
Health impact of acute intermittent porphyria in latent and..:
Buendía-Martínez, Juan
;
Barreda-Sánchez, María
;
Rodríguez-Peña, Lidya
...
Orphanet Journal of Rare Diseases. 16 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1186/..
?
10
High penetrance of acute intermittent porphyria in a Spanis..:
Barreda-Sánchez, María
;
Buendía-Martínez, Juan
;
Glover-López, Guillermo
...
Orphanet Journal of Rare Diseases. 14 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1186/..
?
11
EDA, EDAR, EDARADD and WNT10A allelic variants in patients ..:
GIEDE (Spanish multidisciplinary research group for ectodermal dysplasia)
;
Martínez-Romero, María Carmen
;
Ballesta-Martínez, María Juliana
...
Orphanet Journal of Rare Diseases. 14 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1186/..
?
12
R248G cystic fibrosis transmembrane conductance regulator m..:
Villalona, Seiichi
;
Glover-López, Guillermo
;
Ortega-García, Juan Antonio
...
Journal of Medical Case Reports. 11 (2017) 1 - p. , 2017
Link:
https://doi.org/10.1186/..
?
13
Molecular Testing for Fragile X: Analysis of 5062 Tests fro..:
María-Isabel Tejada
;
Guillermo Glover
;
Francisco Martínez
...
http://dx.doi.org/10.1155/2014/195793. , 2014
Link:
https://doi.org/10.1155/..
?
14
Estudio genético de la porfiria aguda intermitente en la Re..:
Guillén Navarro, Encarnación
;
Glover Lopéz, Guillermo
;
Fernández Barreiro, Andrés
.
http://hdl.handle.net/10201/30761. , 1999
Link:
http://hdl.handle.net/10..
?
15
Estudio molecular del sindrome X frágil / Guillermo Glover ..:
Glover Lopéz, Guillermo
http://hdl.handle.net/10201/34172. , 1992
Link:
http://hdl.handle.net/10..
1-15
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