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UnknownmHealth Assessment: Conceptualization of a Global Framework.
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S-EPMC5434253 | biostudies-literature
UnknownAssessment of Myocardial Microstructural Dynamics by In Vivo Diffusion Tensor Cardiac Magnetic Resonance.
Not available
S-EPMC8672367 | biostudies-literature
UnknownSimultaneous non-contrast assessment of cardiac microstructure and perfusion in vivo in the human heart.
Not available
S-EPMC12182817 | biostudies-literature
UnknownPosterior Polymorphous Corneal Dystrophy in a Patient with a Novel ZEB1 Gene Mutation.
Not available
S-EPMC9820445 | biostudies-literature
UnknownExpanding the Phenotypic Spectrum of PAX6 Mutations: From Congenital Cataracts to Nystagmus.
Not available
S-EPMC8151272 | biostudies-literature
UnknownFamilial imbalance in 16p13.11 leads to a dosage compensation rearrangement in an unaffected carrier.
Not available
S-EPMC4412105 | biostudies-literature
UnknownPartial paternal uniparental disomy (UPD) of chromosome 1 in a patient with Stargardt disease.
Not available
S-EPMC2553007 | biostudies-literature
UnknownOPA1 Dominant Optic Atrophy: Diagnostic Approach in the Pediatric Population.
Not available
S-EPMC9857649 | biostudies-literature
UnknownCIBERER: Spanish national network for research on rare diseases: A highly productive collaborative initiative.
Not available
S-EPMC9305285 | biostudies-literature
UnknownMolecular analysis of ABCA4 and CRB1 genes in a Spanish family segregating both Stargardt disease and autosomal recessive retinitis pigmentosa.
Not available
S-EPMC2258218 | biostudies-literature
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