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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 characterization of a new contiguous gene syndrome
Souza, Josiane, Faucz, Fábio, Sotomaior, Vanessa, Bonalumi Filho, Aguinaldo, Rosenfeld, Jill, Raskin, SalmoVolume:
34
Language:
english
Journal:
Genetics and Molecular Biology
DOI:
10.1590/S1415-47572011005000044
Date:
September, 2011
File:
PDF, 1.08 MB
english, 2011