Carbonic anhydrase II deficiency syndrome with amelogenesis imperfecta linked to a homozygous CA2 deletion

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Autor(es) e Colaborador(es): 
University of Brasilia, University Hospital of Brasilia, Unit of Oral Health, Oral Care Center for Inherited Diseases
University of Brasilia, University Hospital of Brasilia, Unit of Oral Health, Oral Care Center for Inherited Diseases
University of Brasilia, Faculty of Health Sciences, Department of Dentistry, Laboratory of Oral Histopathology
University of Brasilia, Faculty of Medicine, Laboratory of Clinical Genetics
University of Brasilia, University Hospital of Brasilia, Unit of Pediatric Nephrology
University of Brasilia, University Hospital of Brasilia, Unit of Pediatric Nephrology
University of Brasilia, Faculty of Health Sciences, Department of Dentistry, Laboratory of Oral Histopathology
University of Brasilia, University Hospital of Brasilia, Unit of Oral Health, Oral Care Center for Inherited Diseases
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Data: 
31-Out-2024
31-Out-2024
2022
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