Setian, N
2 papers on CoChat
Most cited papers
- Verified
Impact of molecular mechanisms, including deletion size, on Prader-Willi syndrome phenotype: Study of 75 patients
Varela, M., Kok, F., Setian, N., Kim, C., & Koiffmann, C. (2005) · Clinical Genetics
Genetic Syndromes and ImprintingGenomic variations and chromosomal abnormalities
Cited by 117
- Verified
Estudo multicêntrico de pacientes brasileiros com deficiência da 21-hidroxilase: correlação do genótipo com o fenótipo
Bachega, T. A. S. S., Billerbeck, A. E. C., Parente, É. B., Lemos-Marini, S. H. V., Baptista, M. T. M., Mello, M. P., Guerra Jr., G., Kuperman, H., Setian, N., Damiani, D., et al. (2004) · Arquivos Brasileiros de Endocrinologia & Metabologia
Sexual Differentiation and DisordersAdrenal Hormones and Disorders
Cited by 25
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