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Human Mutation|July 22, 1998
Analysis of recurrent germline mutations in the MEN1 gene encountered in apparently unrelated familiesS K Agarwal, L V Debelenko, M B Kester, et al.
Nature Genetics|July 16, 2002
Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndromeKirk Mykytyn, Darryl Y Nishimura, Charles C Searby, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 12, 2019
Integrative analysis of gene expression, DNA methylation, physiological traits, and genetic variation in human skeletal muscleD Leland Taylor, Anne U Jackson, Narisu Narisu, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2025
Genetics of growth rate in induced pluripotent stem cellsBrian N Lee, Henry J Taylor, Filippo Cipriani, et al.
Ebiomedicine|May 21, 2025
Modelling adrenal steroid profiles to inform monitoring guidance in congenital adrenal hyperplasiaNeil R Lawrence, Jeremy Dawson, Zi-Qiang Lang, et al.
American Journal of Human Genetics|May 26, 2021
Genetic effects on liver chromatin accessibility identify disease regulatory variantsKevin W Currin, Michael R Erdos, Narisu Narisu, et al.
Journal of Internal Medicine|July 29, 1998
Germline and somatic mutation of the gene for multiple endocrine neoplasia type 1 (MEN1)S J Marx, S K Agarwal, M B Kester, et al.
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