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Refinado por: Nome da Publicação: American Journal of Human Genetics remover Biblioteca: FMRP - Fac. Medicina de Ribeirão Preto remover
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1
American Journal of Human Genetics
Material Type:
Revista 		Adicionar ao Meu Espaço

American Journal of Human Genetics

UNITED STATES University of Chicago Press etc.

Acesso online. A biblioteca também possui exemplares impressos.

2
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)

3
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)

4
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)

5
Complex chromosome rearrangement (CCR) involving chromosomes 2,5,11, and 16 and a reciprocal translocation between chromosomes 6 and 8 verifled by spectra karyotyping (SKY) in a girl with mlld dysmorphic features and mental retardation
Complex chromosome rearrangement (CCR) involving chromosomes 2,5,11, and 16 and a reciprocal translocation between chromosomes 6 and 8 verifled by spectra karyotyping (SKY) in a girl with mlld dysmorphic features and mental retardation
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Complex chromosome rearrangement (CCR) involving chromosomes 2,5,11, and 16 and a reciprocal translocation between chromosomes 6 and 8 verifled by spectra karyotyping (SKY) in a girl with mlld dysmorphic features and mental retardation

Ester Silveira Ramos S. R Rogatto; Lúcia Regina Martelli; S. A Piram; J. A Squire; Annual Meeting of the American Society of Human Genetics (49. 1999 San Francisco)

American Journal of Human Genetics Baltimore v. 65, n. 4, p. A356 res. 2009, 1999

Baltimore 1999

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1079048 ) e outros locais(Acessar)

6
Methylation of p15 tumor-supressor gene in familial and sporadic malignant melanome
Methylation of p15 tumor-supressor gene in familial and sporadic malignant melanome
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Methylation of p15 tumor-supressor gene in familial and sporadic malignant melanome

Greice Andreotti de Molfetta P. S. P Lima; M. V. S Passos; Wilson Araújo da Silva Júnior; Annual Meeting of the American Society of Human Genetics (53. 2003 Los Angeles)

American Journal of Human Genetics Chicago v. 73, n. 5, supl., p. 250, 2003

Chicago 2003

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1351139 ) e outros locais(Acessar)

7
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)

8
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)

9
Detection of Y-sequences by PCR in patiente with turner stigmata
Detection of Y-sequences by PCR in patiente with turner stigmata
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Detection of Y-sequences by PCR in patiente with turner stigmata

Milena Jorge Simões Flória Lima Santos Rosane Gomes de Paula Queiroz; L. C Caetano; L. H. G Teixeira; Lúcia Regina Martelli; 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. 281 res. 574, 2001

Chicago 2001

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1226245 ) e outros locais(Acessar)

10
Correction mitochondrial DNA variation in amerindians [carta]
Correction mitochondrial DNA variation in amerindians [carta]
Material Type:
Artigo 		Adicionar ao Meu Espaço

Correction mitochondrial DNA variation in amerindians [carta]

Wilson Araújo da Silva Júnior Sandro Luíz Bonatto; Adriano de Jesus Holanda; Andrea K Ribeiro-dos-Santos; Beatriz M Paixão; Gustavo Henrique Goldman; Kiyoko Abe-Sandes; Luis Rodriguez-Delfin; Marcela Barbosa; Maria Luísa Paço-Larson; Maria Luiza Petzl-Erler; Valéria Valente; Sidney Emanuel Batista dos Santos; Marco Antônio Zago

American Journal of Human Genetics Atlanta v. 72, p. 1346-1348, 2003

Atlanta 2003

Localização: FCFRP - Fac. Ciên. Farm. Ribeirão Preto    (pcd 1419730 ) e outros locais(Acessar)

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Deste Autor:

  1. Silva Júnior, W
  2. Zago, M
  3. Santos, S
  4. Ramos, E
  5. Petzl-Erler, M

Neste Assunto:

  1. Genética Médica
  2. Doenças Genéticas
  3. Genética
  4. População
  5. Anomalia Craniofacial

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

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