Cromosoma 13 en anillo

dc.contributor.authorFrancisco Cammarata‐Scalisi
dc.contributor.authorYajaira Briceño
dc.contributor.authorEdymar Cegarra
dc.contributor.authorDaniela Montilla
dc.coverage.spatialBolivia
dc.date.accessioned2026-03-22T17:56:55Z
dc.date.available2026-03-22T17:56:55Z
dc.date.issued2019
dc.description.abstractClinical findings that can guide the diagnosis of this infrequent structural chromosomal alteration are highlighted, as well as the interdisciplinary medical evaluation required and adequate family genetic counseling.
dc.identifier.doi10.24875/bmhim.18000108
dc.identifier.urihttps://doi.org/10.24875/bmhim.18000108
dc.identifier.urihttps://andeanlibrary.org/handle/123456789/67204
dc.language.isoes
dc.publisherElsevier BV
dc.relation.ispartofBoletín Médico del Hospital Infantil de México
dc.sourceUniversidad de Los Andes
dc.subjectMicrocephaly
dc.subjectMedicine
dc.subjectGynecology
dc.subjectPediatrics
dc.titleCromosoma 13 en anillo
dc.typearticle

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