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Glover, Guillermo
341  results:
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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..
 
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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..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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..
 
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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..
 
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