skip to main content
Idioma:
Resultados 1 2 3 4 5 next page
Mostrar Somente
Refinado por: Nome da Publicação: American Journal of Human Genetics remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Clinical and molecular aspects of 25 brazilian Friedreich's patients
Clinical and molecular aspects of 25 brazilian Friedreich's patients
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Clinical and molecular aspects of 25 brazilian Friedreich's patients

Lilian Maria José Albano Mayana Zatz; C. A Kim; D Bertola; Sofia Mizuho Miura Sugayama; Maria Joaquina Marques Dias; Fernando Kok; I Ferrareto; Sérgio Rosemberg; S Cocozza; Alcir José Monticelli; Annual Meeting of the American Society of Human Genetics (2000 Chicago)

American Journal of Human Genetics v. 67, n. 4, suppl. 2, p. 409, outubro 2000

Chicago 2000

Localização: FM - Fac. Medicina    (BCSEP 2000 81 )(Acessar)

2
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)

3
Linkage analysis in a large brazilian family with knobloch syndrome
Linkage analysis in a large brazilian family with knobloch syndrome
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Linkage analysis in a large brazilian family with knobloch syndrome

Maria Rita Passos-Bueno A L Sertie; M Quimby; J Murray; Suely Kazue Nagahashi Marie; M Zatz; Annual Meeting of the American Society of Human Genetics (45. 1995 Minneapolis)

v.57, n.4 suppl., p.a333, oct. 1995 American Journal of Human Genetics

1995

Item não circula. Consulte sua biblioteca.(Acessar)

4
Proteus syndrome with plexiform neurofibromas
Proteus syndrome with plexiform neurofibromas
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Proteus syndrome with plexiform neurofibromas

Claudette Hajaj Gonzalez C A Kim; J C Neto; Osny Salomão; N R B Oliveira; International Congress of Human Genetics (8. 1991 Washington)

v.49, n.4 suppl., p.138, oct. 1991 American Journal of Human Genetics

1991

Localização: FM - Fac. Medicina    (BCSEP 1991 159 ) e outros locais(Acessar)

5
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)

6
Clinical cytogenetical and molecular studies of the Angelman syndrome in 62 Brazilian patients
Clinical cytogenetical and molecular studies of the Angelman syndrome in 62 Brazilian patients
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Clinical cytogenetical and molecular studies of the Angelman syndrome in 62 Brazilian patients

Greice Andreotti de Molfetta V. F Ferraz; W. A Silva Junior; João Monteiro de Pina Neto; Annual Meeting of the American Society of Human Genetics (50. 2000 Philadelphia)

American Journal of Human Genetics Chicago v. 67, n. 4, supl. 2, p. 127, res. 650, 2000

Chicago 2000

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1176600 ) e outros locais(Acessar)

7
'GAMA' - sarcoglycan mutations in lgmd 2c
'GAMA' - sarcoglycan mutations in lgmd 2c
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

'GAMA' - sarcoglycan mutations in lgmd 2c

E M Mcnally C G Bonnemann; D Duggan; J R M Gorospe; Maria Rita Passos-Bueno; Mariz Vainzof; Mayana Zatz; S Noguchi; E Ozawa; E P Hoffman; L M Kunkel; Annual Meeting of the American Society of Human Genetics (46. 1996 San Francisco)

v.59, n.4 suppl., p.a271, 1996 American Journal of Human Genetics

1996

Item não circula. Consulte sua biblioteca.(Acessar)

8
Molecular cytogenetic characterization of an unbalanced t(4p;21q) in a patient misdiagnosed as full monosomy 21
Molecular cytogenetic characterization of an unbalanced t(4p;21q) in a patient misdiagnosed as full monosomy 21
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Molecular cytogenetic characterization of an unbalanced t(4p;21q) in a patient misdiagnosed as full monosomy 21

Lucia Regina Martinelli Ester Silveira Ramos; C. G. C Lemos; V. M Motta; S. A Santos; T. A Bernardes; A. C. C Nassar; J. R Coelho; J. E Chufalo; S Almeida; J. G Franco Junior; Annual Meeting of the American Society of Human Genetics (49. 1999 San Francisco)

American Journal of Human Genetics Baltimore v. 65, n. 4, p. A351 res. 1979, 1999

Baltimore 1999

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1079043 ) e outros locais(Acessar)

9
Retrospective study on the impact of diagnosis and genetic counseling in neuromuscular diseases
Retrospective study on the impact of diagnosis and genetic counseling in neuromuscular diseases
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Retrospective study on the impact of diagnosis and genetic counseling in neuromuscular diseases

S. Eggers Mayana Zatz; R C M Pavanello; International Congress of Human Genetics (8. 1991 Washington)

v.49, n.4 suppl., p.311, oct. 1991 American Journal of Human Genetics

1991

Item não circula. Consulte sua biblioteca.(Acessar)

10
Neuroblastoma in a child with dup 12q23 qter due to maternal translocation with breakpoints on 11q23 and 12q23
Neuroblastoma in a child with dup 12q23 qter due to maternal translocation with breakpoints on 11q23 and 12q23
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Neuroblastoma in a child with dup 12q23 qter due to maternal translocation with breakpoints on 11q23 and 12q23

C. P Koiffmann Claudette Hajaj Gonzalez; D. H Souza; Vicente Odone Filho; C A Kim; D Moretti-Ferreira; Anita Wajntal; International Congress of Human Genetics (8. 1991 Washington)

v.49, n.4 suppl., p.243, oct. 1991 American Journal of Human Genetics

1991

Localização: FM - Fac. Medicina    (BCSEP 1991 159 ) e outros locais(Acessar)

Resultados 1 2 3 4 5 next page

Personalize Seus Resultados

  1. Editar

Refine Search Results

Mostrar Somente

  1. Disponível na Biblioteca (19)

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

Buscando em bases de dados remotas. Favor aguardar.