Extending the phenotype of monosomy 1p36 syndrome and mapping of a critical region for obesity and hyperphagia von D'Angelo, Carla S., Kohl, Ilana, Varela, Monica Castro, de Castro, Cláudia I.E., Kim, Chong A., Bertola, Débora R., Lourenço, Charles M., Koiffmann, Célia P.

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Molecular cytogenetic characterization of an inherited maternal duplication 20p11.21p13 associated with a small 20p11.21 deletion von D'Angelo, Carla S., de Oliveira, Mariana A., de Castro, Claudia I.E., Koiffmann, Celia P.

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A new case of interstitial 6q16.2 deletion in a patient with Prader–Willi-like phenotype and investigation of  SIM1 gene deletion in 87 patients with syndromic obesity von Varela, Monica C., Simões-Sato, Alex Y., Kim, Chong A., Bertola, Débora R., De Castro, Claudia I.E., Koiffmann, Celia P.

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Investigation of selected genomic deletions and duplications in a cohort of 338 patients presenting with syndromic obesity by multiplex ligation-dependent probe amplification using... von D'Angelo, Carla S, Varela, Monica C, de Castro, Cláudia Ie, Kim, Chong A, Bertola, Débora R, Lourenço, Charles M, Perez, Ana Beatriz A, Koiffmann, Celia P

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