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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Disease and BBS9[original query]
Capitalizing on admixture in genome-wide association studies: a two-stage testing procedure and application to height in African-Americans.
Frontiers in genetics 2011 2 .
Kang Guolian, Gao Guimin, Shete Sanjay, Redden David T, Chang Bao-Li, Rebbeck Timothy R, Barnholtz-Sloan Jill S, Pajewski Nicholas M, Allison David
Copy-Number Variation Contributes to the Mutational Load of Bardet-Biedl Syndrome.
American journal of human genetics 2016 Aug 99 (2): 318-36.
Lindstrand Anna, Frangakis Stephan, Carvalho Claudia M B, Richardson Ellen B, McFadden Kelsey A, Willer Jason R, Pehlivan Davut, Liu Pengfei, Pediaditakis Igor L, Sabo Aniko, Lewis Richard Alan, Banin Eyal, Lupski James R, Davis Erica E, Katsanis Nichol
Clinical and exome sequencing findings in seven children with Bardet-Biedl syndrome from Turkey.
Annals of human genetics 2020 7 85 (1): 27-36.
Gumus Evren, Tuncez Ebru, Oz Ozlem, Saka Guvenc Mer
Next Generation Sequencing Identifies Five Novel Mutations in Lebanese Patients with Bardet-Biedl and Usher Syndromes.
Genes 2020 1 10 (12): .
Jaffal Lama, Joumaa Wissam H, Assi Alexandre, Helou Charles, Cherfan George, Zibara Kazem, Audo Isabelle, Zeitz Christina, El Shamieh Sa
Spectrum of pathogenic variants and high prevalence of pathogenic BBS7 variants in Russian patients with Bardet-Biedl syndrome.
Frontiers in genetics 2024 8 15 1419025.
M Orlova, P Gundorova, V Kadnikova, A Polyak
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