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Published in Human reproduction (Oxford) (01.08.2019)
Published in Human reproduction (Oxford) (01.08.2019)
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Genotype FBN1/phenotype relationship in a cohort of patients with Marfan syndrome
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Published in Clinical genetics (01.02.2021)
Published in Clinical genetics (01.02.2021)
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New mutations found by Next-Generation Sequencing screening of Spanish patients with Nemaline Myopathy
Moreau-Le Lan, Sarah, Aller, Elena, Calabria, Ines, Gonzalez-Tarancon, Lola, Cardona-Gay, Cristina, Martinez-Matilla, Marina, Aparisi, Maria J, Selles, Jorge, Sagath, Lydia, Pitarch, Inmaculada, Muelas, Nuria, Cervera, Jose V, Millan, Jose M, Pedrola, Laia
Published in PloS one (05.12.2018)
Published in PloS one (05.12.2018)
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Prenatal Genome-Wide Cell-Free DNA Screening: Three Years of Clinical Experience in a Hospital Prenatal Diagnostic Unit in Spain
Pedrola Vidal, Laia, Roselló Piera, Mónica, Martín-Grau, Carla, Rubio Moll, Juan S, Gómez Portero, Rosa, Marcos Puig, Beatriz, Cervera Zamora, Jose V, Quiroga, Ramiro, Orellana Alonso, Carmen
Published in Genes (28.04.2024)
Published in Genes (28.04.2024)
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De novo erythroleukemia chromosome features include multiple rearrangements, with special involvement of chromosomes 11 and 19
Cigudosa, Juan C., Odero, Maria D., Calasanz, M. José, Solé, Francesc, Salido, Marta, Arranz, Eva, Martínez-Ramirez, Angel, Urioste, Miguel, Alvarez, Sara, Cervera, Jose V., MacGrogan, Donald, Sanz, Miguel A., Nimer, Stephen D., Benitez, Javier
Published in Genes chromosomes & cancer (01.04.2003)
Published in Genes chromosomes & cancer (01.04.2003)
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