Mostrando 1 - 20 Resultados de 184 Para buscar 'Hereditary', tiempo de consulta: 0.06s Limitar resultados
  • 1
    Genotype - phenotype correlation in CADASIL. Cognitive performance in carriers of notch3 mutations R1031C and C455R
    Palabra clave: “...Hereditary vascular dementia...”
    Guardado en:
  • 2
    Genotype - phenotype correlation in CADASIL. Cognitive performance in carriers of notch3 mutations R1031C and C455R
    Palabra clave: “...Hereditary vascular dementia...”
    Guardado en:
  • 3
    Genotype - phenotype correlation in CADASIL. Cognitive performance in carriers of notch3 mutations R1031C and C455R
    Palabra clave: “...Hereditary vascular dementia...”
    Guardado en:
  • 4
    Genotype - phenotype correlation in CADASIL. Cognitive performance in carriers of notch3 mutations R1031C and C455R
    Palabra clave: “...Hereditary vascular dementia...”
    Guardado en:
  • 5
    Genotype - phenotype correlation in CADASIL. Cognitive performance in carriers of notch3 mutations R1031C and C455R
    Palabra clave: “...Hereditary vascular dementia...”
    Guardado en:
  • 6
    Genotype - phenotype correlation in CADASIL. Cognitive performance in carriers of notch3 mutations R1031C and C455R
    Palabra clave: “...Hereditary vascular dementia...”
    Guardado en:
  • 7
    Genotype - phenotype correlation in CADASIL. Cognitive performance in carriers of notch3 mutations R1031C and C455R
    Palabra clave: “...Hereditary vascular dementia...”
    Guardado en:
  • 8
    Genotype - phenotype correlation in CADASIL. Cognitive performance in carriers of notch3 mutations R1031C and C455R
    Palabra clave: “...Hereditary vascular dementia...”
    Guardado en:
  • 9
    Genotype - phenotype correlation in CADASIL. Cognitive performance in carriers of notch3 mutations R1031C and C455R
    Palabra clave: “...Hereditary vascular dementia...”
    Guardado en:
  • 10
    Genotype - phenotype correlation in CADASIL. Cognitive performance in carriers of notch3 mutations R1031C and C455R
    Palabra clave: “...Hereditary vascular dementia...”
    Guardado en:
  • 11
    Genotype - phenotype correlation in CADASIL. Cognitive performance in carriers of notch3 mutations R1031C and C455R
    Palabra clave: “...Hereditary vascular dementia...”
    Guardado en:
  • 12
    Genotype - phenotype correlation in CADASIL. Cognitive performance in carriers of notch3 mutations R1031C and C455R
    Palabra clave: “...Hereditary vascular dementia...”
    Guardado en:
  • 13
    Genotype - phenotype correlation in CADASIL. Cognitive performance in carriers of notch3 mutations R1031C and C455R
    Palabra clave: “...Hereditary vascular dementia...”
    Guardado en:
  • 14
    Genotype - phenotype correlation in CADASIL. Cognitive performance in carriers of notch3 mutations R1031C and C455R
    Palabra clave: “...Hereditary vascular dementia...”
    Guardado en:
  • 15
    Genotype - phenotype correlation in CADASIL. Cognitive performance in carriers of notch3 mutations R1031C and C455R
    Palabra clave: “...Hereditary vascular dementia...”
    Guardado en:
  • 16
    Genotype - phenotype correlation in CADASIL. Cognitive performance in carriers of notch3 mutations R1031C and C455R
    Palabra clave: “...Hereditary vascular dementia...”
    Guardado en:
  • 17
    Síndrome de Rendu Osler Weber en una adolescente en Colombia : reporte de un caso de autopsia.
    Palabra clave: “...telangiectasia hereditary hemorrhagic...”
    Guardado en:
  • 18
    Hipoacusia neurosensorial en el Síndrome de Alport: una revisión sistemática
    Palabra clave: “...Nephritis, Hereditary...”
    Guardado en:
  • 19
    Síndrome dismórfico neonatal: reporte de caso de un diagnóstico severo
    Autores Ismena Cari, Flor, Rojas-Guerra, Roy Jonatan
    Publicado 2024-04-24
    Palabra clave: “...Congenital, Hereditary, and Neonatal Diseases and Abnormalities...”
    Guardado en:
  • 20
    Síndrome dismórfico neonatal: reporte de caso de un diagnóstico severo
    Autores Ismena Cari, Flor, Rojas-Guerra, Roy Jonatan
    Publicado 2024-04-24
    Palabra clave: “...Congenital, Hereditary, and Neonatal Diseases and Abnormalities...”
    Guardado en:
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