Publications by authors named "Ana Pecina"

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Preimplantation Genetic Diagnosis for Myotonic Dystrophy Type 1 and Analysis of the Effect of the Disease on the Reproductive Outcome of the Affected Female Patients.
Raquel María Fernández, María Dolores Lozano-Arana, Beatriz Sánchez, Ana Peciña, Juan Carlos García-Lozano

Biomed Res Int· August 2018

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Clinical and Technical Overview of Preimplantation Genetic Diagnosis for Fragile X Syndrome: Experience at the University Hospital Virgen del Rocio in Spain.
Raquel M Fernández, Ana Peciña, Maria Dolores Lozano-Arana, Beatriz Sánchez, Juan Carlos García-Lozano

Biomed Res Int· September 2016

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Co-segregation of a homozygous SMN1 deletion and a heterozygous PMP22 duplication in a patient.
Raquel M Fernández, Ana Peciña, Beatriz Muñoz-Cabello, Guillermo Antiñolo, Salud Borrego

Clin Case Rep· September 2016

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Experience of Preimplantation Genetic Diagnosis for Hemophilia at the University Hospital Virgen Del Rocío in Spain: Technical and Clinical Overview.
Raquel M Fernández, Ana Peciña, Beatriz Sánchez, Maria Dolores Lozano-Arana, Juan Carlos García-Lozano

Biomed Res Int· May 2016

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Experience of preimplantation genetic diagnosis with HLA matching at the University Hospital Virgen del Rocío in Spain: technical and clinical overview.
Raquel María Fernández, Ana Peciña, Maria Dolores Lozano-Arana, Beatriz Sánchez, Jordi Guardiola

Biomed Res Int· September 2015

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Atypical Association of Angelman Syndrome and Klinefelter Syndrome in a Boy with 47,XXY Karyotype and Deletion 15q11.2-q13.
Javier Sánchez, Ana Peciña, Olga Alonso-Luengo, Antonio González-Meneses, Rocío Vázquez

Case Rep Genet· November 2014

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Novel one-step multiplex PCR-based method for HLA typing and preimplantational genetic diagnosis of β-Thalassemia.
Raquel M Fernández, Ana Peciña, Maria Dolores Lozano-Arana, Juan Carlos García-Lozano, Salud Borrego

Biomed Res Int· December 2013

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One-step multiplex polymerase chain reaction for preimplantation genetic diagnosis of Huntington disease.
Ana Peciña, María Dolores Lozano Arana, Juan C García-Lozano, Salud Borrego, Guillermo Antiñolo

Fertil Steril· May 2010

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Mutation update of spinal muscular atrophy in Spain: molecular characterization of 745 unrelated patients and identification of four novel mutations in the SMN1 gene.
Laura Alías, Sara Bernal, Pablo Fuentes-Prior, María Jesus Barceló, Eva Also

Hum Genet· February 2009

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Analysis of RET polymorphisms and haplotypes in the context of sporadic medullary thyroid carcinoma.
Raquel M Fernández, Ana Peciña, Guillermo Antiñolo, Elena Navarro, Salud Borrego

Thyroid· April 2006

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The RET IVS1-126G>T variant is strongly associated with the development of sporadic medullary thyroid cancer.
R M Fernandez, Mercedes Robledo, Guillermo Antinolo, Ana Pecina, Sergio Ruiz-Llorente

Thyroid· April 2004

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Targeted stimulation of meiotic recombination.
Ana Peciña, Kathleen N Smith, Christine Mézard, Hajime Murakami, Kunihiro Ohta

Cell· October 2002

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