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M L Freckmann

Showing results (1-10 of 4) with videos related to

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Annals of Neurology|July 14, 2000
Leigh disease caused by the mitochondrial DNA G14459A mutation in unrelated familiesD M Kirby, S G Kahler, M L Freckmann, et al.
The Journal of Pediatrics|March 1, 1997
Mitochondrial electron transport chain defect presenting as hypoglycemiaM L Freckmann, D R Thorburn, D M Kirby, et al.
Neurogastroenterology and Motility|May 22, 2018
Variants in ACTG2 underlie a substantial number of Australasian patients with primary chronic intestinal pseudo-obstructionG Ravenscroft, S Pannell, G O'Grady, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 16, 2013
Genotype and clinical care correlations in craniosynostosis: findings from a cohort of 630 Australian and New Zealand patientsT Roscioli, G Elakis, T C Cox, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Annals of Neurology|July 14, 2000
Leigh disease caused by the mitochondrial DNA G14459A mutation in unrelated familiesD M Kirby, S G Kahler, M L Freckmann, et al.
The Journal of Pediatrics|March 1, 1997
Mitochondrial electron transport chain defect presenting as hypoglycemiaM L Freckmann, D R Thorburn, D M Kirby, et al.
Neurogastroenterology and Motility|May 22, 2018
Variants in ACTG2 underlie a substantial number of Australasian patients with primary chronic intestinal pseudo-obstructionG Ravenscroft, S Pannell, G O'Grady, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 16, 2013
Genotype and clinical care correlations in craniosynostosis: findings from a cohort of 630 Australian and New Zealand patientsT Roscioli, G Elakis, T C Cox, et al.
Pageof 1