describing the benefits of knowing your Love DNA for a happier marriage.

Microcephaly: investigation and diagnostic approach 1 Aluno de graduação em medicina no Centro Universitário de Volta Redonda (UniFOA). 2 Aluna de Graduação

ORIGINAL ARTICLEhttps://doi.org/10.1590/1516-3180.2020.0470.R2.110321 Clinical and cytogenetic characteristics of patients diagnosed with Turner syndrome in a clinical genetics

250 Vicente Lopes Monte Neto1 Data de submissão: 02/12/2013. Data de aprovação: 06/02/2014. Correspondência para: Paulo Roberto Santos. Faculdade

Bart syndrome: A case report 1 Physician - Pediatric Resident. Hospital Regional de Mato Grosso do Sul (HRMS), Campo Grande, MS, Brazil. 2 Pediatric Dermatologist (HC-UFPR)

UntitledZurich Open Repository and Archive University of Zurich University Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 2020 A rare urea cycle disorder

PDF hosted at the Radboud Repository of the Radboud University Nijmegen For additional information about this publication click this link. https://hdl.handle.net/2066/220627

Anemia de Fanconi Resumen La anemia de Fanconi es una enfermedad hereditaria con patrón de transmisión au- tosómico recesivo, asociada con múltiples