Browsing by Author Marini, S H
Showing results 1 to 5 of 5
| Preview | Issue Date | Title | Author(s) | Advisor | Type |
| 1999 | Mutation Distribution And Cyp21/c4 Locus Variability In Brazilian Families With The Classical Form Of The 21-hydroxylase Deficiency. | Paulino, L C; Araujo, M; Guerra, G; Marini, S H; De Mello, M P | - | Artigo de periódico |
| 1997 | Female Pseudohermaphroditism Due To Classical 21-hydroxylase Deficiency In A Girl With Turner Syndrome. | Maciel-Guerra, A T; Guerra, G; Marini, S H; Matias Baptista, M T; Marques-de-Faria, A P | - | Artigo de periódico |
| - | True Hermaphrodites In The Southeastern Region Of Brazil: A Different Cytogenetic And Gonadal Profile. | Guerra Júnior, G; de Mello, M P; Assumpção, J G; Morcillo, A M; Marini, S H; Baptista, M T; Paiva e Silva, R B; Marqués-de-Faria, A P; Maciel-Guerra, A T | - | Artigo de periódico |
| 2000 | Turner's Syndrome And Thyroid Disease: A Transverse Study Of Pediatric Patients In Brazil. | Medeiros, C C; Marini, S H; Baptista, M T; Guerra, G; Maciel-Guerra, A T | - | Artigo de periódico |
| 2001 | Family-based Association Of Hla Class Ii Alleles And Haplotypes With Type I Diabetes In Brazilians Reveals Some Characteristics Of A Highly Diversified Population. | Volpini, W M; Testa, G V; Marques, S B; Alves, L I; Silva, M E; Dib, S A; Guerra, G; Paulino, M F; Marini, S H; Persoli, L B; Caillat-Zucman, S | - | Artigo de periódico |
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