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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 - 4 (of 4 Records)

Query Trace: Disease and LRP4[original query]
No mutations in the serotonin related TPH1 and HTR1B genes in patients with monogenic sclerosing bone disorders.
Bone 2013 Jul 55 (1): 52-6.
Boudin Eveline, Jennes Karen, de Freitas Fenna, Tegay David, Mortier Geert, Van Hul W
A common LRP4 haplotype is associated with bone mineral density and hip geometry in men-data from the Odense Androgen Study (OAS).
Bone 2013 Apr 53 (2): 414-20.
Boudin Eveline, Steenackers Ellen, de Freitas Fenna, Nielsen Torben Leo, Andersen Marianne, Brixen Kim, Van Hul Wim, Piters El
Novel polymorphisms associated with hyperalphalipoproteinemia and apparent cardioprotection.
Journal of clinical lipidology 2017 Nov .
Oates Connor P, Koenig Darya, Rhyne Jeffrey, Bogush Nikolay, O'Connell Jeffrey, Mitchell Braxton D, Miller Micha
Mutations in the fourth ?-propeller domain of LRP4 are associated with isolated syndactyly with fusion of the third and fourth fingers.
Human mutation 2018 3 39 (6): 811-815.
Sukenik Halevy Rivka, Chien Huan-Chieh, Heinz Bo, Bamshad Michael J, Nickerson Deborah A, , Kircher Martin, Ahituv Nad
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