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1
American Journal of Human Genetics
Material Type:
Revista 		Añadir a Mi Portal

American Journal of Human Genetics

UNITED STATES University of Chicago Press etc.

Acceso en línea. La biblioteca tiene también copias físicas.

2
Global analysis of gene expression in inherited human craniosinostosis
Global analysis of gene expression in inherited human craniosinostosis
Material Type:
Artículo de Congreso 		Añadir a Mi Portal

Global analysis of gene expression in inherited human craniosinostosis

T. S. Zorick A. Y Fernandes; P Turma; Hamilton Matsushita; Silvio Antonio Zanini; A Palhares; Maria Rita Passos-Bueno; Annual Meeting of the American Society of Human Genetics (51. 2001 San Diego)

American Journal of Human Genetics Chicago v. 69, n. 4, suppl., p. 454, oct. 2001

Chicago 2001

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3
DNMT1 is not required for maintenance of XIST repression in human cancer cells
DNMT1 is not required for maintenance of XIST repression in human cancer cells
Material Type:
Artículo de Congreso 		Añadir a Mi Portal

DNMT1 is not required for maintenance of XIST repression in human cancer cells

Luciana dos Reis Vasques M Soukoyan; Lygia da Veiga Pereira; Annual Meeting of the American Society of Human Genetics (51. 2001 San Diego)

American Journal of Human Genetics Chicago v. 69, n. 4, suppl., p. 373, oct. 2001

Chicago 2001

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4
Human type XVIII collagen (Col18A1) gene structural organization, identification of new SNPs, and its exclusion as the Knobloch syndrome gene
Human type XVIII collagen (Col18A1) gene structural organization, identification of new SNPs, and its exclusion as the Knobloch syndrome gene
Material Type:
Artículo de Congreso 		Añadir a Mi Portal

Human type XVIII collagen (Col18A1) gene structural organization, identification of new SNPs, and its exclusion as the Knobloch syndrome gene

A L Sertie V Sossi; Maria Rita Passos-Bueno; C Brahe; American Society of Human Genetics (49. 1999 San Francisco)

American Journal of Human Genetics Baltimore v. 65, n. 4, suppl., res. 2143, oct. 1999

San Francisco 1999

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5
Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene
Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene
Material Type:
Artículo 		Añadir a Mi Portal

Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene

P Ianakiev M. J van Baren; M. J Daly; S. P. A Toledo (Sérgio Pereira de Almeida); M. G Cavalcanti; J Correia Neto; E. Lemos Silveira; Ademar Freire Maia; P Heutink; M. W Kilpatrick; P Tsipouras

American Journal of Human Genetics v. 68, p. 01-08, 2000

Estados Unidos 2000

Disponible en FM - Fac. Medicina    (BCSEP 2000 81 )(Obténgalo)

6
Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene
Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene
Material Type:
Artículo 		Añadir a Mi Portal

Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene

P. Ianakiev M. J. van Baren; M. J Daly; S. P. A Toledo (Sérgio Pereira de Almeida); M. G Cavalcanti; J Correa Neto; E. Lemos Silveira; A Freire Maia; P Heutink; M. W Kilpatrick; P Tsipouras

American Journal of Human Genetics v. 68, p. 38-45, 2001

Chicago 2001

Disponible en FM - Fac. Medicina    (BCSEP 2001 046 )(Obténgalo)

7
Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene
Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene
Material Type:
Artículo 		Añadir a Mi Portal

Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene

P. Ianakiev M. J. van Baren; M. J Daly; S. P. A Toledo (Sérgio Pereira de Almeida); M. G Cavalcanti; J Correa Neto; E. Lemos Silveira; A Freire Maia; P Heutink; M. W Kilpatrick; P Tsipouras

American Journal of Human Genetics v. 68, p. 38-45, 2001

Chicago 2001

Disponible en FM - Fac. Medicina    (BCSEP 2001 046 )(Obténgalo)

8
A pattent with supernumerary nostril and other anomalies
A pattent with supernumerary nostril and other anomalies
Material Type:
Artículo de Congreso 		Añadir a Mi Portal

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

Disponible en FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1225043 ) y otras localizaciones(Obténgalo)

9
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:
Artículo de Congreso 		Añadir a Mi Portal

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

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10
Sex ratio distribution in latin-america
Sex ratio distribution in latin-america
Material Type:
Artículo de Congreso 		Añadir a Mi Portal

Sex ratio distribution in latin-america

M F Feitosa Henrique Krieger; International Congress of Human Genetics (8. 1991 Washington)

v.49, n.4 suppl., p.473, 1991 American Journal of Human Genetics

1991

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