Human Genome Epidemiology Literature Finder
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Query Trace: Turner Syndrome and MYOD1[original query] |
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A pharmacogenomic approach to the treatment of children with GH deficiency or Turner syndrome. European journal of endocrinology / European Federation of Endocrine Societies 2013 Sep 169 (3): 277-89. Clayton P, Chatelain P, Tatò L, Yoo H W, Ambler G R, Belgorosky A, Quinteiro S, Deal C, Stevens A, Raelson J, Croteau P, Destenaves B, Olivier |
- Page last reviewed:Feb 1, 2024
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