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| Issue Date | Title | Author(s) |
|---|---|---|
| 2012 | A novel DAX1/NR0B1 mutation in a patient with adrenal hypoplasia congenita and hypogonadotropic hypogonadism | BATTISTIN, Claudilene; MENEZES FILHO, Hamilton Cabral de; DOMENICE, Sorahia; NISHI, Mirian Yumie; MANNA, Thais Della; KUPERMAN, Hilton; STEINMETZ, Leandra; DICHTCHEKENIAN, Vae; SETIAN, Nuvarte; DAMIANI, Durval |
| 2012 | Analysis of anti-Mullerian hormone (AMH) and its receptor (AMHR2) genes in patients with persistent Mullerian duct syndrome | NISHI, Mirian Yumie; DOMENICE, Sorahia; MACIEL-GUERRA, Andrea Trevas; ZABA NETO, Alberto; SILVA, Marcia Alessandra Cavalaro Pereira da; COSTA, Elaine Maria Frade; GUERRA-JUNIOR, Gil; MENDONCA, Berenice Bilharinho de |
| 2011 | Clinical and molecular aspects of a pediatric metachronous adrenocortical tumor | LIMA, Lorena de Oliveira; LERARIO, Antonio Marcondes; ALENCAR, Guilherme Asmar; BRITO, Luciana Pinto; ALMEIDA, Madson Queiroz; DOMENICE, Sorahia; LATRONICO, Ana Claudia; MENDONCA, Berenice Bilharinho; FRAGOSO, Maria Candida Barrison Villares |
| 2013 | Y chromosome aberration in a patient with cloacal-bladder exstrophy-epispadias complex: an unusual finding | NISHI, Mirian Yumie; MARTINS, Thais Cotrim; COSTA, Elaine Maria Frade; MENDONCA, Berenice Bilharinho; GIRON, Amilcar Martins; DOMENICE, Sorahia |
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