skip to main content
Idioma:

Resultados de 11 a 20 de 1.039  para Produção Intelectual da USP

Ordenado por: Ordenado por: RelevânciaOr hit Enter to replace sort method
previous page 1 Resultados 2 3 4 5 next page
Mostrar Somente
Refinado por: assunto: Genética Médica remover
Result Number Material Type Add to My Shelf Action Record Details and Options
11
A pattent with supernumerary nostril and other anomalies
A pattent with supernumerary nostril and other anomalies
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

A pattent with supernumerary nostril and other anomalies

J. Huber José Batista Volpon; Ester Silveira Ramos; Annual Meeting of the American Society of Human Genetics (2001 Chicago)

American Journal of Human Genetics Chicago v. 69, p. 290 res. 624, 2001

Chicago 2001

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1225043 ) e outros locais(Acessar)

12
Spectral Karyotyping study of three patients with constitutional supernumerary chromossomal markers
Spectral Karyotyping study of three patients with constitutional supernumerary chromossomal markers
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Spectral Karyotyping study of three patients with constitutional supernumerary chromossomal markers

Ester Silveira Ramos Lúcia Regina Martelli; J Karaskowa; J Huber; L. D. R Giuliani; Beatriz R Versiani; Maria Lúcia Machado; Lucimar A. F Laureano; J Squire; European Human Genetics Conference (2002 Strasbourg); European Meeting on Psychosocial Aspects of Genetics (2002 Strasbourg)

European Journal of Human Genetics London v. 10, supl. 1, p. 132, res. P0273, 2002

2002

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1294955 ) e outros locais(Acessar)

13
Heterozygosity probabilities for normal relatives of isolated cases affected by incompletely penetrant dominant conditions
Heterozygosity probabilities for normal relatives of isolated cases affected by incompletely penetrant dominant conditions
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Heterozygosity probabilities for normal relatives of isolated cases affected by incompletely penetrant dominant conditions

Paulo A Otto S R P Maestrelli; International Congress of Human Genetics (8. 1991 Washington)

v.49, n.4 suppl., p.489, oct. 1991 American Journal of Human Genetics

1991

Item não circula. Consulte sua biblioteca.(Acessar)

14
Insensitivity androgen syndrome associated with microcephaly mental deficiency and hypoplasy of fourth metatarsi case report
Insensitivity androgen syndrome associated with microcephaly mental deficiency and hypoplasy of fourth metatarsi case report
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Insensitivity androgen syndrome associated with microcephaly mental deficiency and hypoplasy of fourth metatarsi case report

C. Vretos P. L Takeuchi; F. C Dolabella; L. C Caetano; Silvio Tucci Júnior; Ester Silveira Ramos; Annual Meeting of The American Society of Human Genetics (54. 2004 Toronto)

Abstracts Bethesda: American Society of Human Genetics, 2004

Bethesda American Society of Human Genetics 2004

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1421767 ) e outros locais(Acessar)

15
Association of the polymorphism IGF2/Apal with birth weight and body mass index
Association of the polymorphism IGF2/Apal with birth weight and body mass index
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Association of the polymorphism IGF2/Apal with birth weight and body mass index

M. V. M. Gomes M. R Soares; C. R Marcondes; A Pasqualim-Neto; Raysildo Barbosa Lôbo; Ester Silveira Ramos; Annual Meeting of The American Society of Human Genetics (54. 2004 Toronto)

Abstracts Bethesda: American Society of Human Genetics, 2004

Bethesda American Society of Human Genetics 2004

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1421956 ) e outros locais(Acessar)

16
Molecular cytogenetic analysis of a ring chromosome 15
Molecular cytogenetic analysis of a ring chromosome 15
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Molecular cytogenetic analysis of a ring chromosome 15

S. R. Pereira-Martins Lucia Regina Martelli; D G Mello; C L Bassi; M L Machado; M A A Salles; Ester Silveira Ramos; Annual Meeting of the American Society of Human Genetics (1998 Chicago)

American Journal of Human Genetics Chicago v. 63, n. 4 supl., p. A147 res. 829, 1998

Chicago 1998

Item não circula. Consulte sua biblioteca.(Acessar)

17
Population stratification assessment and genomic control in Brazilian Head and Neck Squamous cell carcinoma (HNSCC) patients
Population stratification assessment and genomic control in Brazilian Head and Neck Squamous cell carcinoma (HNSCC) patients
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Population stratification assessment and genomic control in Brazilian Head and Neck Squamous cell carcinoma (HNSCC) patients

L. F. Araújo M. R Luizon; G. A Molfetta; C. A Ferreira; A. A Marques; A. K Ribeiro-Santos; S. E Santos; Wilson Araújo da Silva Júnior; European Human Genetics Conference (2012 London)

European Journal of Humana Genetics London v. 20, suppl.1, p. 162, res. P.10.46, 2012

London 2012

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2401001 estantes deslizantes ) e outros locais(Acessar)

18
Mutation analysis of UBE3A gene in Angelman syndrome patients
Mutation analysis of UBE3A gene in Angelman syndrome patients
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Mutation analysis of UBE3A gene in Angelman syndrome patients

G. A. Molfetta W. A Silva Júnior; J Wagstalf; João Monteiro de Pina Neto; Annual Meeting of the American Journal of Human Genetics (2001 Chicago)

American Journal of Human Genetics Chicago v. 69, n. 4, p. 580 res. 2345, 2001

Chicago 2001

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1226236 ) e outros locais(Acessar)

19
Molecular approach in the study of idiopathic infertile male
Molecular approach in the study of idiopathic infertile male
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Molecular approach in the study of idiopathic infertile male

E L Sartorato R C Carrara; W O Bragança; R Yamasaki; C Hackel; João Monteiro de Pina Neto; Annual Meeting of the American Society of Human Genetics (1998 Chicago)

American Journal of Human Genetics Chicago v. 63, n. 4 supl., p. A384 res. 2227, 1998

Chicago 1998

Item não circula. Consulte sua biblioteca.(Acessar)

20
Lacunar skull and limb defect with 22q11 microdeletion novel feature of velocario-facial syndrome ?
Lacunar skull and limb defect with 22q11 microdeletion novel feature of velocario-facial syndrome ?
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Lacunar skull and limb defect with 22q11 microdeletion novel feature of velocario-facial syndrome ?

S. E. Hansing P. S Garcia; D. D Rosa; Maria Lúcia Machado; Geraldo Aleixo Silva Passos; Ester Silveira Ramos; Annual Meeting of the American Journal of Human Genetics (2001 Chicago)

American Journal of Human Genetics Chicago v. 69, n. 4, p. 305, res. 714, 2001

Chicago 2001

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1226249 ) e outros locais(Acessar)

Resultados de 11 a 20 de 1.039  para Produção Intelectual da USP

Ordenado por: Ordenado por: RelevânciaOr hit Enter to replace sort method
previous page 1 Resultados 2 3 4 5 next page

Personalize Seus Resultados

  1. Editar

Refine Search Results

Mostrar Somente

  1. Disponível na Biblioteca (320)
  2. Recursos Online (31)

Refinar Meus Resultados

Tipo de Recurso 

  1. Artigos  (999)
  2. Produções Acadêmicas  (35)
  3. Livros  (4)
  4. Mais opções open sub menu

Data de Publicação 

De até
Refinar
  1. Antes de1992  (114)
  2. 1992Até1999  (603)
  3. 2000Até2007  (191)
  4. 2008Até2016  (76)
  5. Após 2016  (56)
  6. Mais opções open sub menu

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

Buscando em bases de dados remotas. Favor aguardar.