Maíra Cristina Menezes Freire

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Infantile myofibromatosis (IM) is a rare disorder characterized by the development of benign tumors in the skin, muscle, bone, and viscera. The incidence is 1/150,000 live births and the disease is(More)
The assessment of nucleotide polymorphisms in environmental samples of obligate pathogens requires DNA amplification through the polymerase chain reaction (PCR) and bacterial cloning of PCR products(More)
In 2014 we published in the European Journal of Medical Genetics the article entitled “Exome sequencing identifies a novel homozygous variant in NDRG4 in a family with infantile myofibromatosis”(More)
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