Dra. Lívia Polisseni
Médica Geneticista
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Cartão de Visitas
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Read 16p11.2 microduplication syndrome report
Read 16p11.2 microduplication syndrome report
We report the first case of a child with 16p11.2 microduplication syndrome with increased fluid in the cisterna magna seen on magnetic resonance imaging (MRI).
Explore syndrome analysis in genetics
Explore syndrome analysis in genetics
What is the definition of Syndrome? Since the beginning of studies in genetics, certain terminologies have been created and used to define groups of diseases or alterations. With the advancement of k...
Read about glucose-galactose malabsorption
Read about glucose-galactose malabsorption
Congenital glucose-galactose malabsorption (CGGM) is a rare metabolic disorder caused by a deficient intestinal sodium-dependent glucose cotransporter…
Currículo Lattes
Currículo Lattes
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