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Sports (Basel, Switzerland)|September 25, 2019
Running Propensities of Athletes with Hamstring InjuriesDai Sugimoto, Brian D Kelly, David L Mandel, et al.Lancet (London, England)|May 6, 1995
Rapid antibody test for fragile X syndromeR Willemsen, S Mohkamsing, B de Vries, et al.Open Access Emergency Medicine : OAEM|February 28, 2020
The Impact of a Concierge Medicine Model on Door to Doctor Time and Patient Flow in an Urban Emergency DepartmentAsher L Mandel, Thomas Bove, Amisha D Parekh, et al.Nature|December 12, 1996
Mutations in the kinase Rsk-2 associated with Coffin-Lowry syndromeE Trivier, D De Cesare, S Jacquot, et al.Journal of Cardiac Surgery|November 24, 2022
An alternate approach: Percutaneous axillary cannulation for minimally invasive cardiac surgeryJenna L Mandel, Colin C Yost, Jake L Rosen, et al.Proceedings of the National Academy of Sciences of the United States of America|January 1, 1984
Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus)G Camerino, K H Grzeschik, M Jaye, et al.European Journal of Human Genetics : EJHG|October 22, 1998
Genomic organization of the MTM1 gene implicated in X-linked myotubular myopathyJ Laporte, C Guiraud-Chaumeil, S M Tanner, et al.Nature|February 25, 1993
Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transportersJ Mosser, A M Douar, C O Sarde, et al.Nature Genetics|June 1, 1996
A gene mutated in X-linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeastJ Laporte, L J Hu, C Kretz, et al.American Journal of Medical Genetics|April 1, 1992
Methylation and mutation patterns in the fragile X syndromeH Malmgren, M L Steén-Bondeson, K H Gustavson, et al.Pageof 31