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Molecular Medicine Reports|November 14, 2013
Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334‑kb deletion: a case reportIoannis Papoulidis, Eirini Oikonomidou, Sandro Orru, et al.Haematologica|March 28, 2008
Comparative genome profiling across subtypes of low-grade B-cell lymphoma identifies type-specific and common aberrations that target genes with a role in B-cell neoplasiaBibiana I Ferreira, Juan F García, Javier Suela, et al.The American Journal of Pathology|June 19, 2010
Deregulated expression of the polycomb-group protein SUZ12 target genes characterizes mantle cell lymphomaDaniel Martín-Pérez, Esther Sánchez, Lorena Maestre, et al.Revista De Neurologia|December 15, 2015
[Phenotypic variability of the 1q21.1 microdeletion syndrome in members of the same family: relevance of detection of neuropsychiatric disorders for diagnosis of genetic syndromes]Daniel Natera-De Benito, Arantxa Vidal-Esteban, Jaime Sanchez-Del Pozo, et al.American Journal of Medical Genetics. Part A|August 28, 2010
Molecular characterization of a new patient with a non-recurrent inv dup del 2q and review of the mechanisms for this rearrangementAscensión Vera-Carbonell, Isabel López-Expósito, Juan Antonio Bafalliu, et al.Transplant International : Official Journal of the European Society for Organ Transplantation|February 26, 2005
Expression of adhesion molecules and RANTES in kidney transplant from nonheart-beating donorsManuel Gomez del Moral, Beatriz Aviles, Ingrid K Colberger, et al.Journal of Medical Genetics|June 4, 2024
Guidelines for NGS procedures applied to prenatal diagnosis by the Spanish Society of Gynecology and Obstetrics and the Spanish Association of Prenatal DiagnosisAnna Abulí, Eugenia Antolín, Antoni Borrell, et al.American Journal of Medical Genetics. Part A|July 30, 2013
A 2.84 Mb deletion at 21q22.11 in a patient clinically diagnosed with Marden-Walker syndromeMaría Carmen Carrascosa-Romero, Javier Suela, José Manuel Pardal-Fernández, et al.Medicina Clinica|February 25, 2017
Recommendations for the use of microarrays in prenatal diagnosisJavier Suela, Isabel López-Expósito, María Eugenia Querejeta, et al.American Journal of Medical Genetics. Part A|May 1, 2014
Microduplication 10q24.31 in a Spanish girl with scoliosis and myopathy: the critical role of LBXAlberto Fernández-Jaén, Javier Suela, Daniel Martín Fernández-Mayoralas, et al.Pageof 3