skip to main content
Idioma:
previous page 1 Resultados 2 3 next page
Refinado por: Nome da Publicação: American Journal Of Human Genetics remover assunto: Biological And Medical Sciences remover
Result Number Material Type Add to My Shelf Action Record Details and Options
11
Discovery and Fine Mapping of Serum Protein Loci through Transethnic Meta-analysis
Discovery and Fine Mapping of Serum Protein Loci through Transethnic Meta-analysis
Material Type:
Artigo 		Adicionar ao Meu Espaço

Discovery and Fine Mapping of Serum Protein Loci through Transethnic Meta-analysis

FRANCESCHINI, Nora ; VAN ROOIJ, Frank J. A ; BAUMERT, Jens ; BORASKA, Vesna ; BROER, Linda ; HAYWARD, Caroline ; NGWA, Julius S ; OKADA, Yukinori ; POLASEK, Ozren ; WESTRA, Harm-Jan ; WANG, Ying A ; DEL GRECO M, Fabiola ; PRINS, Bram P ; GLAZER, Nicole L ; KAPUR, Karen ; KEMA, Ido P ; LOPEZ, Lorna M ; SCHILLERT, Arne ; SMITH, Albert V ; WINKLER, Cheryl A ; ZGAGA, Lina ; BANDINELLI, Stefania ; BERGMANN, Sven ; FEITOSA, Mary F ; BOBAN, Mladen ; BOCHUD, Murielle ; CHEN, Y. D ; DAVIES, Gail ; DEHGHAN, Abbas ; JINGZHONG DING ; DOERING, Angela ; DURDA, J. Peter ; FERRUCCI, Luigi ; FRANCO, Oscar H ; KARAKAS, Mahir ; FRANKE, Lude ; GUNJACA, Grog ; HOFMAN, Albert ; HSU, Fang-Chi ; KOLCIC, Ivana ; KRAJA, Aldi ; KUBO, Michiaki ; LACKNER, Karl J ; LAUNER, Lenore ; LOEHR, Laura R ; ECKFELDT, John H ; GUO LI ; MEISINGER, Christa ; NAKAMURA, Yusuke ; SCHWIENBACHER, Christine ; STARR, John M ; TAKAHASHI, Atsushi ; TORLAK, Vesela ; UITTERLINDEN, Andre G ; VITART, Veronique ; WALDENBERGER, Melanie ; FOLSOM, Aaron R ; KOPP, Jeffrey ; VAEZ, Ahmad ; ANDREWS, Jeanette S

American journal of human genetics, 2012-10, Vol.91 (4), p.744-753 [Periódico revisado por pares]

Cambridge, MA: Cell Press

Texto completo disponível

Citações Citado por
12
Linkage disequilibrium in the region of the autosomal dominant polycystic kidney disease gene (PKD1)
Linkage disequilibrium in the region of the autosomal dominant polycystic kidney disease gene (PKD1)
Material Type:
Artigo 		Adicionar ao Meu Espaço

Linkage disequilibrium in the region of the autosomal dominant polycystic kidney disease gene (PKD1)

SNAREY, A ; THOMAS, S ; FRISCHAUF, A.-M ; SCHNEIDER, M. C ; POUND, S. E ; BARTON, N ; WRIGHT, A. F ; SOMLO, S ; GERMINO, G. G ; HARRIS, P. C ; REEDERS, S. T

American journal of human genetics, 1994-08, Vol.55 (2), p.365-371 [Periódico revisado por pares]

Chicago, IL: University of Chicago Press

Texto completo disponível

Citações Citado por
13
Transformation of Sib-Pair Values for the Haseman-Elston Method
Transformation of Sib-Pair Values for the Haseman-Elston Method
Material Type:
Artigo 		Adicionar ao Meu Espaço

Transformation of Sib-Pair Values for the Haseman-Elston Method

Wang, Daolong ; Lin, Shili ; Cheng, Rong ; Gao, Xin ; Wright, Fred A.

American journal of human genetics, 2001-05, Vol.68 (5), p.1238-1249 [Periódico revisado por pares]

Chicago, IL: Elsevier Inc

Texto completo disponível

Citações Citado por
14
Heterogeneity analysis in 40 X-linked retinitis pigmentosa families
Heterogeneity analysis in 40 X-linked retinitis pigmentosa families
Material Type:
Artigo 		Adicionar ao Meu Espaço

Heterogeneity analysis in 40 X-linked retinitis pigmentosa families

TEAGUE, P. W ; ALDRED, M. A ; BUNDEY, S ; JAY, B ; BIRD, A. C ; BHATTACHARYA, S. S ; WRIGHT, A. F ; JAY, M ; DEMPSTER, M ; HARRISON, C ; CAROTHERS, A. D ; HARDWICK, L. J ; EVANS, H. J ; STRAIN, L ; BROCK, D. J. H

American journal of human genetics, 1994-07, Vol.55 (1), p.105-111 [Periódico revisado por pares]

Chicago, IL: University of Chicago Press

Texto completo disponível

Citações Citado por
15
A recombination outside the BB deletion refines the location of the X-linked retinitis pigmentosa locus RP3
A recombination outside the BB deletion refines the location of the X-linked retinitis pigmentosa locus RP3
Material Type:
Artigo 		Adicionar ao Meu Espaço

A recombination outside the BB deletion refines the location of the X-linked retinitis pigmentosa locus RP3

FUJITA, R ; BINGHAM, E ; WRIGHT, A. F ; OTT, J ; SIEVING, P. A ; SWAROOP, A ; FORSYTHE, P ; MCHENRY, C ; AITA, V ; NAVIA, B. A ; DRY, K ; SEGAL, M ; DEVOTO, M ; BRUNS, G

American journal of human genetics, 1996-07, Vol.59 (1), p.152-158 [Periódico revisado por pares]

Chicago, IL: University of Chicago Press

Texto completo disponível

Citações Citado por
16
Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another : confirmation of genetic heterogeneity
Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another : confirmation of genetic heterogeneity
Material Type:
Artigo 		Adicionar ao Meu Espaço

Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another : confirmation of genetic heterogeneity

LESTER, D. H ; INGLEHEARN, C. F ; BASHIR, R ; ACKFORD, H ; ESAKOWITZ, L ; JAY, M ; BIRD, A. C ; WRIGHT, A. F ; PAPIHA, S. S ; BHATTACHARYA, S. S

American journal of human genetics, 1990-09, Vol.47 (3), p.536-541 [Periódico revisado por pares]

Chicago, IL: University of Chicago Press

Texto completo disponível

Citações Citado por
17
A Founding Locus within the RET Proto-Oncogene May Account for a Large Proportion of Apparently Sporadic Hirschsprung Disease and a Subset of Cases of Sporadic Medullary Thyroid Carcinoma
A Founding Locus within the RET Proto-Oncogene May Account for a Large Proportion of Apparently Sporadic Hirschsprung Disease and a Subset of Cases of Sporadic Medullary Thyroid Carcinoma
Material Type:
Artigo 		Adicionar ao Meu Espaço

A Founding Locus within the RET Proto-Oncogene May Account for a Large Proportion of Apparently Sporadic Hirschsprung Disease and a Subset of Cases of Sporadic Medullary Thyroid Carcinoma

Borrego, Salud ; Wright, Fred A. ; Fernández, Raquel M. ; Williams, Nita ; López-Alonso, Manuel ; Davuluri, Ramana ; Antiñolo, Guillermo ; Eng, Charis

American journal of human genetics, 2003-01, Vol.72 (1), p.88-100 [Periódico revisado por pares]

Chicago, IL: Elsevier Inc

Texto completo disponível

Citações Citado por
18
Linkage relationships between X-linked retinitis pigmentosa and nine-short-arm markers: exclusion of the disease locus from Xp21 and localization to between DX57 and DX514
Linkage relationships between X-linked retinitis pigmentosa and nine-short-arm markers: exclusion of the disease locus from Xp21 and localization to between DX57 and DX514
Material Type:
Artigo 		Adicionar ao Meu Espaço

Linkage relationships between X-linked retinitis pigmentosa and nine-short-arm markers: exclusion of the disease locus from Xp21 and localization to between DX57 and DX514

WRIGHT, A. F ; BHATTACHARYA, S. S ; CLAYTON, J. F ; DEMPSTER, M ; TIPPETT, P ; MCKEOWN, C. M. E ; JAY, M ; JAY, B ; BIRD, A. C

American journal of human genetics, 1987, Vol.41 (4), p.635-644 [Periódico revisado por pares]

Chicago, IL: University of Chicago Press

Texto completo disponível

Citações Citado por
19
Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
Material Type:
Artigo 		Adicionar ao Meu Espaço

Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans

Medland, Sarah E. ; Nyholt, Dale R. ; Painter, Jodie N. ; McEvoy, Brian P. ; McRae, Allan F. ; Zhu, Gu ; Gordon, Scott D. ; Ferreira, Manuel A.R. ; Wright, Margaret J. ; Henders, Anjali K. ; Campbell, Megan J. ; Duffy, David L. ; Hansell, Narelle K. ; Macgregor, Stuart ; Slutske, Wendy S. ; Heath, Andrew C. ; Montgomery, Grant W. ; Martin, Nicholas G.

American journal of human genetics, 2009-11, Vol.85 (5), p.750-755 [Periódico revisado por pares]

Cambridge, MA: Elsevier Inc

Texto completo disponível

Citações Citado por
20
GWAS Findings for Human Iris Patterns: Associations with Variants in Genes that Influence Normal Neuronal Pattern Development
GWAS Findings for Human Iris Patterns: Associations with Variants in Genes that Influence Normal Neuronal Pattern Development
Material Type:
Artigo 		Adicionar ao Meu Espaço

GWAS Findings for Human Iris Patterns: Associations with Variants in Genes that Influence Normal Neuronal Pattern Development

Larsson, Mats ; Duffy, David L. ; Zhu, Gu ; Liu, Jimmy Z. ; Macgregor, Stuart ; McRae, Allan F. ; Wright, Margaret J. ; Sturm, Richard A. ; Mackey, David A. ; Montgomery, Grant W. ; Martin, Nicholas G. ; Medland, Sarah E.

American journal of human genetics, 2011-08, Vol.89 (2), p.334-343 [Periódico revisado por pares]

Cambridge, MA: Elsevier Inc

Texto completo disponível

Citações Citado por
previous page 1 Resultados 2 3 next page

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

Buscando em bases de dados remotas. Favor aguardar.