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Refinado por: Nome da Publicação: American Journal of Human Genetics remover assunto: Humans remover
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A High-Density Admixture Map for Disease Gene Discovery in African Americans
A High-Density Admixture Map for Disease Gene Discovery in African Americans
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A High-Density Admixture Map for Disease Gene Discovery in African Americans

Smith, Michael W. ; Patterson, Nick ; Lautenberger, James A. ; Truelove, Ann L. ; McDonald, Gavin J. ; Waliszewska, Alicja ; Kessing, Bailey D. ; Malasky, Michael J. ; Scafe, Charles ; Le, Ernest ; De Jager, Philip L. ; Mignault, Andre A. ; Yi, Zeng ; de Thé, Guy ; Essex, Myron ; Sankalé, Jean-Louis ; Moore, Jason H. ; Poku, Kwabena ; Phair, John P. ; Goedert, James J. ; Vlahov, David ; Williams, Scott M. ; Tishkoff, Sarah A. ; Winkler, Cheryl A. ; De La Vega, Francisco M. ; Woodage, Trevor ; Sninsky, John J. ; Hafler, David A. ; Altshuler, David ; Gilbert, Dennis A. ; O’Brien, Stephen J. ; Reich, David

American journal of human genetics, 2004-05, Vol.74 (5), p.1001-1013 [Periódico revisado por pares]

Chicago, IL: Elsevier Inc

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2
Methods for High-Density Admixture Mapping of Disease Genes
Methods for High-Density Admixture Mapping of Disease Genes
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Methods for High-Density Admixture Mapping of Disease Genes

Patterson, Nick ; Hattangadi, Neil ; Lane, Barton ; Lohmueller, Kirk E. ; Hafler, David A. ; Oksenberg, Jorge R. ; Hauser, Stephen L. ; Smith, Michael W. ; O’Brien, Stephen J. ; Altshuler, David ; Daly, Mark J. ; Reich, David

American journal of human genetics, 2004-05, Vol.74 (5), p.979-1000 [Periódico revisado por pares]

Chicago, IL: Elsevier Inc

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3
Both Rare and Common Polymorphisms Contribute Functional Variation at CHGA, a Regulator of Catecholamine Physiology
Both Rare and Common Polymorphisms Contribute Functional Variation at CHGA, a Regulator of Catecholamine Physiology
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Both Rare and Common Polymorphisms Contribute Functional Variation at CHGA, a Regulator of Catecholamine Physiology

Wen, Gen ; Mahata, Sushil K. ; Cadman, Peter ; Mahata, Manjula ; Ghosh, Sajalendu ; Mahapatra, Nitish R. ; Rao, Fangwen ; Stridsberg, Mats ; Smith, Douglas W. ; Mahboubi, Payam ; Schork, Nicholas J. ; O’Connor, Daniel T. ; Hamilton, Bruce A.

American journal of human genetics, 2004-02, Vol.74 (2), p.197-207 [Periódico revisado por pares]

Chicago, IL: Elsevier Inc

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4
Markers for Mapping by Admixture Linkage Disequilibrium in African American and Hispanic Populations
Markers for Mapping by Admixture Linkage Disequilibrium in African American and Hispanic Populations
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Markers for Mapping by Admixture Linkage Disequilibrium in African American and Hispanic Populations

Smith, Michael W. ; Lautenberger, James A. ; Shin, Hyoung Doo ; Chretien, Jean-Paul ; Shrestha, Sadeep ; Gilbert, Dennis A. ; O’Brien, Stephen J.

American journal of human genetics, 2001-11, Vol.69 (5), p.1080-1094 [Periódico revisado por pares]

Chicago, IL: Elsevier Inc

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5
Ethnic-affiliation estimation by use of population-specific DNA markers
Ethnic-affiliation estimation by use of population-specific DNA markers
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Ethnic-affiliation estimation by use of population-specific DNA markers

SHRIVER, M. D ; SMITH, M. W ; JIN, L ; MARCINI, A ; AKEY, J. M ; DEKA, R ; FERRELL, R. E

American journal of human genetics, 1997-04, Vol.60 (4), p.957-964 [Periódico revisado por pares]

Chicago, IL: University of Chicago Press

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6
Significant Admixture Linkage Disequilibrium across 30 cM around the FY Locus in African Americans
Significant Admixture Linkage Disequilibrium across 30 cM around the FY Locus in African Americans
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Significant Admixture Linkage Disequilibrium across 30 cM around the FY Locus in African Americans

Lautenberger, James A. ; Stephens, J. Claiborne ; O'Brien, Stephen J. ; Smith, Michael W.

American journal of human genetics, 2000-03, Vol.66 (3), p.969-978 [Periódico revisado por pares]

Chicago, IL: Elsevier Inc

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7
Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients
Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients
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Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients

Ensenauer, Regina E. ; Adeyinka, Adewale ; Flynn, Heather C. ; Michels, Virginia V. ; Lindor, Noralane M. ; Dawson, D. Brian ; Thorland, Erik C. ; Lorentz, Cindy Pham ; Goldstein, Jennifer L. ; McDonald, Marie T. ; Smith, Wendy E. ; Simon-Fayard, Elba ; Alexander, Alan A. ; Kulharya, Anita S. ; Ketterling, Rhett P. ; Clark, Robin D. ; Jalal, Syed M.

American journal of human genetics, 2003-11, Vol.73 (5), p.1027-1040 [Periódico revisado por pares]

Chicago, IL: Elsevier Inc

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8
Dermal patterns of 18 and D1 trisomics
Dermal patterns of 18 and D1 trisomics
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Dermal patterns of 18 and D1 trisomics

UCHIDA, I A ; PATAU, K ; SMITH, D W

American journal of human genetics, 1962-12, Vol.14 (4), p.345-352 [Periódico revisado por pares]

United States

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9
Partial-trisomy syndromes. I. Sturge-Weber's disease
Partial-trisomy syndromes. I. Sturge-Weber's disease
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Partial-trisomy syndromes. I. Sturge-Weber's disease

PATAU, K ; THERMAN, E ; SMITH, D W ; INHORN, S L ; PICKEN, B F

American journal of human genetics, 1961-09, Vol.13 (3), p.287-298 [Periódico revisado por pares]

United States

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10
Difficulties in the Estimation of Ethnic Affiliation
Difficulties in the Estimation of Ethnic Affiliation
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Difficulties in the Estimation of Ethnic Affiliation

Brenner, Charles H.

American journal of human genetics, 1998-06, Vol.62 (6), p.1558-1560 [Periódico revisado por pares]

United States: Elsevier Inc

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