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Browsing by Author Marini, SHVL

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Preview	Issue Date	Title	Author(s)	Advisor	Type
	1997	Female pseudohermaphroditism due to classical 21-hydroxylase deficiency in a girl with Turner syndrome	MacielGuerra, AT; Guerra, G; Marini, SHVL; Baptista, MTM; MarquesdeFaria, AP	-	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, WMG; Testa, GV; Marques, SBD; Alves, LI; Silva, MER; Dib, SA; Guerra, G; Paulino, MFVM; Marini, SHVL; Persoli, LBL; Caillat-Zucman, S	-	Artigo de periódico
	2000	Gonadotropin-independent precocious puberty due to luteinizing hormone receptor mutations in Brazilian boys: A novel constitutively activating mutation in the first transmembrane helix	Latronico, AC; Shinozaki, H; Guerra, G; Pereira, MAA; Marini, SHVL; Baptista, MTM; Arnhold, IJP; Fanelli, F; Mendonca, BB; Segaloff, DL	-	Artigo de periódico
	2011	Social skills in women with Turner Syndrome	Suzigan, LZ; Silva, RBDE; Guerra, G; Marini, SHVL; Maciel-Guerra, AT	-	Artigo de periódico
	1999	Mutation distribution and CYP21/C4 locus variability in Brazilian families with the classical form of the 21-hydroxylase deficiency	Paulino, LC; Araujo, M; Guerra, G; Marini, SHVL; De Mello, MP	-	Artigo de periódico

Showing results 1 to 5 of 5