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Antiñolo Gil, Guillermo
187
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Online (187)
Mediatypes
Articles (Online) (114)
OpenAccess-fulltext (73)
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1
ChIP-Seq-Based Approach in Mouse Enteric Precursor Cells Re..:
Villalba Benito, Leticia
;
Torroglosa, Ana
;
Luzón-Toro, Berta
...
International Journal of Molecular Sciences, 21 (23), 1-14.. , 2024
Link:
https://idus.us.es/handl..
?
2
CIBERER: Spanish national network for research on rare dise..:
Luque, Juan
;
Mendes, Ingrid
;
Gómez, Beatriz
...
Clinical Genetics, 101 (5-6), 481-493.. , 2023
Link:
https://idus.us.es/handl..
?
3
Listeriosis outbreak caused by contaminated stuffed pork, A..:
Fernández Martínez, Nicolás Francisco
;
Ruiz Montero, Rafael
;
Briones, Eduardo
...
Eurosurveillance, 27 (43), 9-20.. , 2023
Link:
https://idus.us.es/handl..
?
4
Ex-Utero Intrapartum Treatment (EXIT): indications and outc..:
García Díaz, Lutgardo
;
Agustín, Juan Carlos de
;
Pavón, Antonio
.
BMC Pregnancy and Childbirth, 20 (1), 1-6.. , 2023
Link:
https://idus.us.es/handl..
?
5
Genome-wide analysis of DNA methylation in Hirschsprung ent..:
Villalba-Benito, Leticia
;
López-López, Daniel
;
Torroglosa, Ana
...
Clinical Epigenetics, 13 (1).. , 2022
Link:
https://idus.us.es/handl..
?
6
The utility of Next Generation Sequencing for molecular dia..:
Vidal, Silvia
;
Brandi, Núria
;
Pacheco, Paola
...
Scientific Reports, 11 (1), 18146.. , 2022
Link:
https://idus.us.es/handl..
?
7
Unusual clinical phenotype of Stargardt disease:
Molina-Solana, Pedro
;
Morillo-Sánchez, María José
;
Méndez-Vidal, Cristina
...
Arquivos Brasileiros de Oftalmologia, 84 (4), 391-394.. , 2022
Link:
https://idus.us.es/handl..
?
8
Genetic landscape of 6089 inherited retinal dystrophies aff..:
Perea-Romero, Irene
;
Gordo, Gema
;
Iancu, Ionut F
...
Scientific Reports, 11 (1).. , 2022
Link:
https://idus.us.es/handl..
?
9
Mode of delivery, perinatal outcome and neurodevelopment in..:
Chimenea Toscano, Ángel
;
García Díaz, Lutgardo
;
Antiñolo Gil, Guillermo
BMC Pregnancy and Childbirth, 22 (1), 154-12.. , 2022
Link:
https://idus.us.es/handl..
?
10
CIBERER : Spanish national network for research on rare dis..:
Luque, Juan A
;
Mendes, Ingrid
;
Gómez, Beatriz
...
Clinical Genetics. , 2022
Link:
https://ddd.uab.cat/reco..
?
11
RMRP, RMST, FTX and IPW: novel potential long non-coding RN..:
Luzón-Toro, Berta
;
Villalba Benito, Leticia
;
Fernández, Raquel María
...
ORPHANET JOURNAL OF RARE DISEASES, 16 (4). , 2022
Link:
https://idus.us.es/handl..
?
12
A comprehensive WGS-based pipeline for the identification o..:
González del Pozo, María
;
Fernández Suárez, Elena
;
Bravo Gil, Nereida Inés
...
NPJ GENOMIC MEDICINE, 7 (1), 1-15.. , 2022
Link:
https://idus.us.es/handl..
?
13
CSVS, a crowdsourcing database of the Spanish population ge..:
Peña-Chilet, María
;
Roldán, Gema
;
Perez-Florido, Javier
...
NUCLEIC ACIDS RESEARCH, 49 (D1), 1130-1137.. , 2022
Link:
https://idus.us.es/handl..
?
14
Identification of a PROM1 mutation in a Spanish family with..:
Llavero-Valero, Pilar
;
Morillo-Sánchez, María José
;
Bravo-Gil, Nereida
...
Open Ophthalmology Journal, 15 (1), 314-317.. , 2022
Link:
https://idus.us.es/handl..
?
15
X-linked Retinoschisis Associated with Retinitis Punctata A..:
de Borja Domínguez-Serrano, Francisco
;
Soto-Sierra, Marina
;
González-del Pozo, María
...
The Open Ophthalmology Journal. 15 (2021) 1 - p. 201-205 , 2021
Link:
https://doi.org/10.2174/..
1-15