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American Journal of Medical Genetics|July 27, 2001
Severe lactic acidosis caused by a novel frame-shift mutation in mitochondrial-encoded cytochrome c oxidase subunit IIL J Wong, P Dai, D Tan, et al.Journal of Inherited Metabolic Disease|July 23, 2003
Two adult galactosaemia females with normal ovarian function and identical GALT mutations (Q188R/R333G)W G Ng, Y K Xu, L J Wong, et al.American Journal of Medical Genetics|December 5, 2000
Clinical heterogeneity in mitochondrial DNA deletion disorders: a diagnostic challenge of Pearson syndromeF Lacbawan, C J Tifft, N L Luban, et al.Climacteric : the Journal of the International Menopause Society|June 5, 2020
Health information needs of 1000 midlife Singaporean womenJ L J Wong, W P P Thu, C W Lim, et al.Pakistan Journal of Biological Sciences : PJBS|June 3, 2015
Termite digestomes as a potential source of symbiotic microbiota for lignocelluloses degradation: a reviewL J Wong, P S H'ng, S Y Wong, et al.JIMD Reports|February 15, 2015
Pathologic Variants of the Mitochondrial Phosphate Carrier SLC25A3: Two New Patients and Expansion of the Cardiomyopathy/Skeletal Myopathy Phenotype With and Without Lactic AcidosisE J Bhoj, M Li, R Ahrens-Nicklas, et al.American Journal of Human Genetics|October 1, 1995
Genetic basis of glycogen storage disease type 1a: prevalent mutations at the glucose-6-phosphatase locusK J Lei, Y T Chen, H Chen, et al.Journal of Medical Genetics|February 4, 2009
Infantile cardiomyopathy caused by a mutation in the overlapping region of mitochondrial ATPase 6 and 8 genesS M Ware, N El-Hassan, S G Kahler, et al.Clinical Genetics|October 16, 2016
FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndromeH Dai, V W Zhang, A W El-Hattab, et al.Hypertension (Dallas, Tex. : 1979)|July 25, 2000
Combinations of variations in multiple genes are associated with hypertensionS M Williams, J H Addy, J A Phillips, et al.Pageof 7