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1
Number of CAG repeats in Exon 1 of androgen receptor gene is not related to gender identity in adult patients with male psudohermaphroditism and male transexualism
Number of CAG repeats in Exon 1 of androgen receptor gene is not related to gender identity in adult patients with male psudohermaphroditism and male transexualism
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Number of CAG repeats in Exon 1 of androgen receptor gene is not related to gender identity in adult patients with male psudohermaphroditism and male transexualism

Elaine M. F. Costa Ana Elisa C Billerbeck; Rosana Rocha; Karla F Melo; Tania A. S. S Bachega; Regina M Martin; Elisa D. R. U Verduguez; Ivo J. P Arnhold; Marlene Inacio; Berenice B Mendonça; ENDO - The Endocrine Society's Annual Meeting (85. 2003 Philadelphia)

Resumos Philadelphia p. 622, res. P3-618, 2003

Philadelphia 2003

Localização: FM - Fac. Medicina    (BCSEP 2003 198 ) e outros locais(Acessar)

2
Male pseudohermaphroditism due to 17"beta"-hydroxysteroid dehydrogenase 3 deficiency diagnosis, psychological evaluation, and management
Male pseudohermaphroditism due to 17"beta"-hydroxysteroid dehydrogenase 3 deficiency diagnosis, psychological evaluation, and management
Material Type:
Artigo 		Adicionar ao Meu Espaço

Male pseudohermaphroditism due to 17"beta"-hydroxysteroid dehydrogenase 3 deficiency diagnosis, psychological evaluation, and management

Berenice Bilharinho de Mendonça Marlene Inacio; Ivo Jorge Prado Arnhold; Elaine Maria Frade Costa; Walter Bloise; Regina M Martin; Francisco Tibor Denes; Frederico Arnaldo de Queirós e Silva; Stefan Andersson; Annika Lindqvist; Jean D Wilson

Medicine Philadelphia v. 79, n. 5, p. 299-309, 2000

Philadelphia 2000

Item não circula. Consulte sua biblioteca.(Acessar)

3
An unusual phenotype in a male patient with Frasier syndrome due to IVS9DS+4C>T mutation perineal hypospadias
An unusual phenotype in a male patient with Frasier syndrome due to IVS9DS+4C>T mutation perineal hypospadias
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

An unusual phenotype in a male patient with Frasier syndrome due to IVS9DS+4C>T mutation perineal hypospadias

Karla F. S. Melo R. M Martin; E. M. F Costa; A. A Jorge; Ivo Jorge Prado Arnhold; Berenice Bilharinho de Mendonça; Reunión de la Sociedad Latinoamericana de Investigación Pediátrica (38.); Reunión de la Sociedad Latinoamericana de Endocrinologia Pediátrica (14.)

Tierra del Fuego, 2000

Tierra del Fuego 2000

Localização: FM - Fac. Medicina    (BCSEP 2000 334 )(Acessar)

4
An unusual phenotype in a male patient with frasler syndrome dueto IVS9DS+4C>T mutation perineal hypospadias
An unusual phenotype in a male patient with frasler syndrome dueto IVS9DS+4C>T mutation perineal hypospadias
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

An unusual phenotype in a male patient with frasler syndrome dueto IVS9DS+4C>T mutation perineal hypospadias

Karla F. S. Melo Regina M Martin; Elaine Maria Frade Costa; Alexander A Jorge; Ivo Jorge Prado Arnhold; Berenice Bilharinho de Mendonça; Annual Meeting of the Endocrine Society's (82. 2000 Toronto)

Toronto 2000

Localização: FM - Fac. Medicina    (BCSEP 2000 170 )(Acessar)

5
An unusual phenotype of fraiser syndrome due to IVS9 +4C>T mutation in the WT1 gene predominantly male ambiguous genitalia and absence of gonadal dysgenesis
An unusual phenotype of fraiser syndrome due to IVS9 +4C>T mutation in the WT1 gene predominantly male ambiguous genitalia and absence of gonadal dysgenesis
Material Type:
Artigo 		Adicionar ao Meu Espaço

An unusual phenotype of fraiser syndrome due to IVS9 +4C>T mutation in the WT1 gene predominantly male ambiguous genitalia and absence of gonadal dysgenesis

Karla F. S. Melo Regina M Martin; Elaine M. F Costa; Filomena Carvalho; Alexander A Jorge; Ivo J. P Arnhold; Berenice B Mendonça

The Journal of Clinical Endocrinology & Metabolism Bethesda v. 87, n. 6, p. 2500-2505, 2002

Bethesda 2002

Item não circula. Consulte sua biblioteca.(Acessar)

6
An unusual phenotype of fraiser syndrome due to IVS9 +4C>T mutation in the WT1 gene predominantly male ambiguous genitalia and absence of gonadal dysgenesis
An unusual phenotype of fraiser syndrome due to IVS9 +4C>T mutation in the WT1 gene predominantly male ambiguous genitalia and absence of gonadal dysgenesis
Material Type:
Artigo 		Adicionar ao Meu Espaço

An unusual phenotype of fraiser syndrome due to IVS9 +4C>T mutation in the WT1 gene predominantly male ambiguous genitalia and absence of gonadal dysgenesis

Karla F. S. Melo Regina M Martin; Elaine M. F Costa; Filomena Carvalho; Alexander A Jorge; Ivo J. P Arnhold; Berenice B Mendonça

The Journal of Clinical Endocrinology & Metabolism Bethesda v. 87, n. 6, p. 2500-2505, 2002

Bethesda 2002

Item não circula. Consulte sua biblioteca.(Acessar)

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Deste Autor:

  1. Mendonça, B
  2. Arnhold, I
  3. Costa, E
  4. Martin, R
  5. Melo, K

Neste Assunto:

  1. Endocrinologia
  2. Medicina Interna
  3. Anatomia Patológica
  4. Pseudo-Hermafroditismo
  5. Cirurgia

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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