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Fernandes, A.M., Rocha-Braz, M.G.M., França, M.M., Lerario, A.M., Simões, V.R.F., Zanardo, E.A., Kulikowski, L.D., Martin, R.M., Mendonca, B.B., Ferraz-de-Souza, B.
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Published in Osteoporosis international (01.07.2020)
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Identification of the first homozygous 1‐bp deletion in GDF9 gene leading to primary ovarian insufficiency by using targeted massively parallel sequencing
França, M.M., Funari, M.F.A., Nishi, M.Y., Narcizo, A.M., Domenice, S., Costa, E.M.F., Lerario, A.M., Mendonca, B.B.
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Published in Clinical genetics (01.02.2018)
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PDX1 ‐MODY and dorsal pancreatic agenesis: New phenotype of a rare disease
Caetano, L.A., Santana, L.S., Costa‐Riquetto, A.D., Lerario, A.M., Nery, M., Nogueira, G.F., Ortega, C.D., Rocha, M.S., Jorge, A.A.L., Teles, M.G.
Published in Clinical genetics (01.02.2018)
Published in Clinical genetics (01.02.2018)
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