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Greizy López
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Greizy López
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Greizy López
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Frecuencia de mutaciones en el gen de la usherina (USH2A) en 26 individuos colom...
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Caracterización fenotípica de la retinitis pigmentaria asociada a sordera
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Caracterización fenotípica y molecular de una familia colombiana con fenilcetonu...
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Related Subjects
Arctic medicine. Tropical medicine
Medicine
R
RC955-962
Colombia
DNA mutational analysis
Genetics
Phenylketonurias
Usher syndromes/genetics
diagnóstico clínico
diet
early diagnosis
fenotipo
genetics
hearing loss
intellectual disability
mutation
phenylalanine hydroxylase
pérdida auditiva
retinitis pigmentaria
retinitis pigmentosa
sensorineural
síndromes de usher
trastornos sordoceguera
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