Showing results (21-30 of 118) with videos related to
Sort By:
Pageof 12
Journal of Medical Genetics|December 1, 1986
Molecular deletion analysis in Duchenne muscular dystrophyN S Thomas, P N Ray, R G Worton, et al.Journal of Medical Genetics|August 1, 1997
Monozygotic twins discordant for Aicardi syndromeT Costa, W Greer, G Rysiecki, et al.Journal of Intellectual Disability Research : JIDR|December 7, 2011
Caregiver and adult patient perspectives on the importance of a diagnosis of 22q11.2 deletion syndromeG Costain, E W C Chow, P N Ray, et al.Molecular and Cellular Biology|January 1, 1990
Molecular and functional analysis of the muscle-specific promoter region of the Duchenne muscular dystrophy geneH J Klamut, S B Gangopadhyay, R G Worton, et al.American Journal of Medical Genetics|May 30, 1998
FGFR2 mutation associated with clinical manifestations consistent with Antley-Bixler syndromeK Chun, J Siegel-Bartelt, D Chitayat, et al.The EMBO Journal|December 1, 1991
Molecular analysis of X-autosome translocations in females with Duchenne muscular dystrophyS E Bodrug, J J Holden, P N Ray, et al.Journal of Medical Microbiology|October 22, 2004
Distribution of espI among clinical enterohaemorrhagic and enteropathogenic Escherichia coli isolatesRosanna Mundy, Claire Jenkins, Jun Yu, et al.Frontiers in Immunology|June 14, 2024
Manipulating regulatory T cells: is it the key to unlocking effective immunotherapy for pancreatic ductal adenocarcinoma?Henry Smith, Edward Arbe-Barnes, Enas Abu Shah, et al.Nucleic Acids Research|April 15, 1997
A muscle-specific enhancer within intron 1 of the human dystrophin gene is functionally dependent on single MEF-1/E box and MEF-2/AT-rich sequence motifsH J Klamut, L O Bosnoyan-Collins, R G Worton, et al.American Journal of Medical Genetics|January 1, 1991
Autosomal recessive inheritance of vasopressin-resistant diabetes insipidusJ M Langley, J W Balfe, T Selander, et al.Pageof 12