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Chromosome 19p13.3 deletion in a child with Peutz-Jeghers syndrome, congenital heart defect, high myopia, learning difficulties and dysmorphic features: clinical and molecular char... by Josiane Souza, Fábio Faucz, Vanessa Sotomaior, Aguinaldo Bonalumi Filho, Jill Rosenfeld, Salmo Raskin
Published 2011-01-01
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