skip to main content
Idioma:
Mostrar solo
Refinado por: autor: Santos, M eliminar materia: Transtornos Gonadais eliminar
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Absence of mutations in TCF21 and DHH in Brazilian patients with 46,XY disorders of gonadal development
Absence of mutations in TCF21 and DHH in Brazilian patients with 46,XY disorders of gonadal development
Material Type:
Artículo de Congreso 		Añadir a Mi Portal

Absence of mutations in TCF21 and DHH in Brazilian patients with 46,XY disorders of gonadal development

C. R. Gomes S Domenice; M. A. G Santos; B. B Mendonça; E. M. F Costa; Simpósio "Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do HC-FMUSP" (3. 2007 São Paulo)

Clinics São Paulo v. 62, suppl. 3, p. S92, res. 552, 2007

São Paulo 2007

Disponible en FM - Fac. Medicina    (FM BCBIB ) y otras localizaciones(Obténgalo)

2
Absence of mutations in MDRT1 in patients with 46,xy disorder of sexual developmenta (DSD) due to gonodal dysgenesis
Absence of mutations in MDRT1 in patients with 46,xy disorder of sexual developmenta (DSD) due to gonodal dysgenesis
Material Type:
Artículo de Congreso 		Añadir a Mi Portal

Absence of mutations in MDRT1 in patients with 46,xy disorder of sexual developmenta (DSD) due to gonodal dysgenesis

T E Silva E M F Costa; M G Santos; M Y Nishi; A Z Machado; C R Gomes; M P Brandão; Berenice Bilharinho de Mendonça; Simpósio "Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do Hospital das Clínicas da FMUSP" (4. 2010 São Paulo, SP); Symposium "Advances in Medical Research of the Medical Investigation Laboratories of Hospital das Clínicas da Faculdade de Medicina da USP" (4. 2010 São Paulo, SP)

Clinics São Paulo v. 65, supl.6, p. S75, res. 85, 2010

São Paulo 2010

Disponible en FM - Fac. Medicina    (BCBIB 2010 ) y otras localizaciones(Obténgalo)

3
Absence of inactivating mutations in FGF9 and FGFR2, genes 46,XY patients with disorders of sex development (DSD) due to gonodal dysgenesis
Absence of inactivating mutations in FGF9 and FGFR2, genes 46,XY patients with disorders of sex development (DSD) due to gonodal dysgenesis
Material Type:
Artículo de Congreso 		Añadir a Mi Portal

Absence of inactivating mutations in FGF9 and FGFR2, genes 46,XY patients with disorders of sex development (DSD) due to gonodal dysgenesis

A Z Machado M G Santos; E M F Costa; Berenice Bilharinho de Mendonça; C R Gomes; M P Brandão; M Y Nishi; R B Silva; S Domenice; Simpósio "Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do Hospital das Clínicas da FMUSP" (4. 2010 São Paulo, SP); Symposium "Advances in Medical Research of the Medical Investigation Laboratories of Hospital das Clínicas da Faculdade de Medicina da USP" (4. 2010 São Paulo, SP)

Clinics São Paulo v. 65, supl.6, p. S66, res. 88, 2010

São Paulo 2010

Comprobar fondos(Obténgalo)

4
Inactivating muttations in SF1/NR5A1 do not impair gonadotropin production in 46,XY patients with disorders of sex development (DSD)
Inactivating muttations in SF1/NR5A1 do not impair gonadotropin production in 46,XY patients with disorders of sex development (DSD)
Material Type:
Artículo de Congreso 		Añadir a Mi Portal

Inactivating muttations in SF1/NR5A1 do not impair gonadotropin production in 46,XY patients with disorders of sex development (DSD)

S Domenice A Z Machado; M G Santos; C A Hohl; Patricia Spara Gadelha; M P Brandão; R V Correa; V S Lando; E M F Costa; Berenice Bilharinho de Mendonça; Simpósio "Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do Hospital das Clínicas da FMUSP" (4. 2010 São Paulo, SP); Symposium "Advances in Medical Research of the Medical Investigation Laboratories of Hospital das Clínicas da Faculdade de Medicina da USP" (4. 2010 São Paulo, SP)

Clinics São Paulo v. 65, supl.6, p. S62, res. 74, 2010

São Paulo 2010

Disponible en FM - Fac. Medicina    (BCBIB 2010 ) y otras localizaciones(Obténgalo)

5
Absence of mutations in the promoter and coding regions of STRA8 gene in patients with 46,XX disorders of gonadal development
Absence of mutations in the promoter and coding regions of STRA8 gene in patients with 46,XX disorders of gonadal development
Material Type:
Artículo de Congreso 		Añadir a Mi Portal

Absence of mutations in the promoter and coding regions of STRA8 gene in patients with 46,XX disorders of gonadal development

Mariza A. G. Santos Mirian Y Nishi; Camila Gomes; Sorahia Domenice; Berenice B Mendonça; Elaine M. F Costa; European Society for Paediatric Endocrinology (ESPE) 2008) Turquia (47.

Hormone Research Basel v. 70, suppl. 1, p. 193, res. P2-d3-648, 2008

Basel 2008

Disponible en FM - Fac. Medicina    (BCSEP 219 2008 )(Obténgalo)

6
Seven novel mutations in steroidogenic factor-1 (SF1/NR5A1) in 46,NY DSD patients
Seven novel mutations in steroidogenic factor-1 (SF1/NR5A1) in 46,NY DSD patients
Material Type:
Artículo de Congreso 		Añadir a Mi Portal

Seven novel mutations in steroidogenic factor-1 (SF1/NR5A1) in 46,NY DSD patients

A Z Machado M G Santos; S Domenice; V S Lando; M P Brandão; M Y Nishi; E M F Costa; B Ferraz-de-Souza; J C Achermann; Berenice Bilharinho de Mendonça; Simpósio "Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do Hospital das Clínicas da FMUSP" (4. 2010 São Paulo, SP); Symposium "Advances in Medical Research of the Medical Investigation Laboratories of Hospital das Clínicas da Faculdade de Medicina da USP" (4. 2010 São Paulo, SP)

Clinics São Paulo v. 65, supl.6, p. S66, res. 89, 2010

São Paulo 2010

Disponible en FM - Fac. Medicina    (BCBIB 2010 ) y otras localizaciones(Obténgalo)

Personalizar los resultados

  1. Editar

Refine Search Results

Ampliar mis resultados

  1.   

Mostrar solo

  1. Disponible (5)

  • Realización: ABCD-USP USP   Logos de Redes Sociales: Freepik

Buscando en bases de datos remotas, por favor espere

  • Buscando por
  • enscope:(USP_VIDEOS),scope:("PRIMO"),scope:(USP_FISICO),scope:(USP_EREVISTAS),scope:(USP),scope:(USP_EBOOKS),scope:(USP_PRODUCAO),primo_central_multiple_fe
  • Mostrar lo que tiene hasta ahora