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| Issue Date | Title | Author(s) |
|---|---|---|
| 2016 | The Frequency of Pathogenic Copy Number Variants in Children with Short Stature of Unknown Etiology | CANTON, A.; HOMMA, T.; FURUYA, T.; ROELA, R.; ARNHOLD, I; JORGE, A. |
| 2015 | Analysis of the MKRN3 Promoter Region in Patients with GNRH-Dependent Pubertal Disorder | MACEDO, D.; BESSA, D.; ABREU, A.; BRITO, V.; JORGE, A.; KAISER, U.; LATRONICO, A. |
| 2018 | Genetic Causes of Short Stature in Patients with Previously Diagnosed as Idiopathic Prenatal Short Stature | HOMMA, Thais; FREIRE, B.; FUNARI, M.; LERARIO, M.; MALAQUIAS, A.; JORGE, A. |
| 2015 | A Homozygous Point Mutation in the GH1 Promoter (-161T > C) Leads to Reduced GH Expression in Siblings with Isolated GH Deficiency (IGHD) | CARVALHO, L.; MADEIRA, J.; MARTIN, R.; MONTENEGRO, L.; FRANCA, M.; COSTALONGA, E.; CORREA, F.; OTTO, A.; ARNHOLD, I; FREITAS, H.; MACHADO, U.; MENDONCA, B.; JORGE, A. |
| 2015 | Children with Noonan and Noonan-Like Syndromes Had a Lipid Profile Resembling Metabolic Syndrome and Type 2 Diabetes | MALAQUIAS, A.; HOMMA, T.; MORAES, M.; FUNARI, M.; PEREIRA, A.; VILLARES, S.; BERTOLA, D.; JORGE, A. |
| 2015 | Copy Number Variants in Patients with Congenital Hypopituitarism Associated with Complex Phenotypes | CORREA, F.; FRANCA, M.; CANTON, A.; OTTO, A.; COSTALONGA, E.; BRITO, V; CARVALHO, L.; COSTA, S.; ARNHOLD, I; JORGE, A.; ROSENBERG, C.; MENDONCA, B. |
| 2015 | Whole Exome Sequencing Identifies Genetic Causes of Disproportional Short Stature | VASQUES, G.; FUNARI, M.; LERARIO, A.; FREIRE, B.; SHINJO, S.; MARIE, S.; ARNHOLD, I; JORGE, A. |
| 2018 | Genetic Evaluation of Syndromic Short Stature Children Born Small for Gestational Age | HOMMA, T.; FREIRE, B.; HONJO, R.; DAUBER, A.; FUNARI, M.; LERARIO, A.; ARNHOLD, I.; CANTON, A.; SUGAYAMA, S.; BERTOLA, D.; KIM, C.; MALAQUIAS, A.; JORGE, A. |
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