Jaime Cruz-Rojo

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Department of Genetics, Department of Pediatrics, Division of Endocrinology, 12 de Octubre Hospital, Madrid and Molecular Genetics Laboratory, Research Unit, Hospital Txagorritxu, Vitoria-Gasteiz,(More)
INTRODUCTION 1q21.1 microdeletion syndrome is a caused by a recurrent deletion of the 1q21.1 copy-number variant, which spans 800 kb and includes at least seven genes. It is associated with a(More)
Clinical Characterization of a Girl With Trisomy 20q13.2qter and Monosomy 13q33.1qter: Delineating Phenotype–Genotype Correlations Oihana Belar, Jaime Sanchez del Pozo, Marta Moreno-Garc ıa, Jaime(More)
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