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    Retinitis pigmentosa
    <img src="http://projectbritain.com/images/uk.jpg" width="40" height="20">ENGLISH <i> Retinitis pigmentosa (RP) is a group of inherited retinal disorders that could lead to profou...
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    Foxg1research logo 171x179
    WHAT IS FOXG1? FOXG1 is a rare genetic mutation of the FOXG1 gene that impacts brain development and function. This severe neurological condition is characterized by seizures, inabi...
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    Imagen1
    Research project: How a better characterization of the genotype-phenotype relation will help in applying early symptomatic treatments for Steinert Myotonic Dystrophy patients OVER...
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    Nevus pointing child
    The congenital melanocytic nevus (CMN) is a generally sporadic malformation of the skin, due to mutations that take place during pregnancy. The mutant cells spread and proliferate be...
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