Publications by authors named "Ramiro Quiroga"

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Population-based genetic carrier screening. A consensus statement from the Spanish societies: AEGH, AEDP, ASEBIR, SEAGEN, SEF and SEGCD.
Xavier Vendrell, Anna Abulí, Clara Serra, Juan José Guillén, Joaquín Rueda, Ramiro Quiroga

Eur J Hum Genet· April 2025

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Prenatal Genome-Wide Cell-Free DNA Screening: Three Years of Clinical Experience in a Hospital Prenatal Diagnostic Unit in Spain.
Laia Pedrola Vidal, Mónica Roselló Piera, Carla Martín-Grau, Juan S Rubio Moll, Rosa Gómez Portero, Ramiro Quiroga

Genes (Basel)· April 2024

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Expanding the phenotype of PIGP deficiency to multiple congenital anomalies-hypotonia-seizures syndrome.
Carla Martín-Grau, Carmen Orellana Alonso, Mónica Roselló Piera, Laia Pedrola Vidal, Roberto Llorens-Salvador, Ramiro Quiroga

Clin Genet· August 2023

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Effect of GnRH agonist before IVF on outcomes in infertile endometriosis patients: a randomized controlled trial.
Elisabet Rodríguez-Tárrega, Ana M Monzo, Ramiro Quiroga, Patrocinio Polo-Sánchez, Pedro Fernández-Colom

Reprod Biomed Online· October 2020

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Fetal arthrogryposis secondary to a giant maternal uterine leiomyoma.
José María Vila-Vives, Juan José Hidalgo-Mora, Inmaculada Soler, Juan Rubio, Ramiro Quiroga

Case Rep Obstet Gynecol· December 2012

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Duplication of the Williams-Beuren critical region: case report and further delineation of the phenotypic spectrum.
C Orellana, Jordi Bernabeu, Sandra Monfort, Monica Rosello, Juan Silvestre Oltra, Ramiro Quiroga

BMJ Case Rep· November 2011

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Enrichment of ultraconserved elements among genomic imbalances causing mental delay and congenital anomalies.
Francisco Martínez, Sandra Monfort, Mónica Roselló, Silvestre Oltra, David Blesa, Ramiro Quiroga

BMC Med Genomics· November 2010

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Prenatal study of common submicroscopic "genomic disorders" using MLPA with subtelomeric/microdeletion syndrome probe mixes, among gestations with ultrasound abnormalities in the first trimester.
Mónica Roselló, Irene Ferrer-Bolufer, Sandra Monfort, Silvestre Oltra, Ramiro Quiroga

Eur J Med Genet· July 2010

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Tyrosinemia type 1 and Angelman syndrome due to paternal uniparental isodisomy 15.
Irene Ferrer-Bolufer, Jaime Dalmau, Ramiro Quiroga, Silvestre Oltra, Carmen Orellana

J Inherit Metab Dis· December 2009

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