Showing results (251-260 of 317) with videos related to
Sort By:
Pageof 32
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.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.Nature|December 12, 1996
Mutations in the kinase Rsk-2 associated with Coffin-Lowry syndromeE Trivier, D De Cesare, S Jacquot, 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.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.Clinical Chemistry|June 3, 1999
A two-year study of microscopic urinalysis competency using the urinalysis-review computer programM L Astion, S Kim, A Nelson, et al.Nature Genetics|May 1, 1995
Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated formY Trottier, D Devys, G Imbert, et al.Nature Genetics|February 1, 1995
Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer proteinK Ouahchi, M Arita, H Kayden, et al.Pageof 32