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Proceedings of the National Academy of Sciences of the United States of America
|
October 19, 2011
Iron deficiency drives an autosomal dominant hypophosphatemic rickets (ADHR) phenotype in fibroblast growth factor-23 (Fgf23) knock-in mice
Emily G Farrow, Xijie Yu, Lelia J Summers, et al.
Molecular and Cellular Biology
|
March 7, 2007
Molecular insights into the klotho-dependent, endocrine mode of action of fibroblast growth factor 19 subfamily members
Regina Goetz, Andrew Beenken, Omar A Ibrahimi, et al.
American Journal of Medical Genetics. Part A
|
September 19, 2009
Skeletal abnormalities in neurofibromatosis type 1: approaches to therapeutic options
Florent Elefteriou, Mateusz Kolanczyk, Aaron Schindeler, et al.
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of 11
Search research articles
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Showing results (101-110 of 103) with videos related to
Sort By:
Page
of 11
You have reached the last page of results.
This site can display upto 103 results.
Proceedings of the National Academy of Sciences of the United States of America
|
October 19, 2011
Iron deficiency drives an autosomal dominant hypophosphatemic rickets (ADHR) phenotype in fibroblast growth factor-23 (Fgf23) knock-in mice
Emily G Farrow, Xijie Yu, Lelia J Summers, et al.
Molecular and Cellular Biology
|
March 7, 2007
Molecular insights into the klotho-dependent, endocrine mode of action of fibroblast growth factor 19 subfamily members
Regina Goetz, Andrew Beenken, Omar A Ibrahimi, et al.
American Journal of Medical Genetics. Part A
|
September 19, 2009
Skeletal abnormalities in neurofibromatosis type 1: approaches to therapeutic options
Florent Elefteriou, Mateusz Kolanczyk, Aaron Schindeler, et al.
Page
of 11