Browsing by Author Marini, S H

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PreviewIssue DateTitleAuthor(s)AdvisorType
1997Female 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
1999Mutation 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
2001Family-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
2000Turner'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
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