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Oral Diseases|January 16, 2009
Enamel defects and salivary methylmalonate in methylmalonic acidemiaC W Bassim, J T Wright, J P Guadagnini, et al.AJNR. American Journal of Neuroradiology|September 6, 2014
MRI characteristics of globus pallidus infarcts in isolated methylmalonic acidemiaE H Baker, J L Sloan, N S Hauser, et al.Blood Cells, Molecules & Diseases|January 1, 1996
Localization of the hemochromatosis disease gene: linkage disequilibrium analysis using an American patient collectionN K Seese, C P Venditti, K A Chorney, et al.Behavior Genetics|March 1, 1994
DNA markers associated with high versus low IQ: the IQ Quantitative Trait Loci (QTL) ProjectR Plomin, G E McClearn, D L Smith, et al.Journal of Medical Genetics|January 1, 1997
46,XX, inv(6)(p21.1p23) in a pedigree with hereditary haemochromatosisC P Venditti, N K Seese, G S Gerhard, et al.American Journal of Medical Genetics|July 1, 1993
Clinical and molecular analyses of deletion 3p25-pter syndromeP N Mowrey, M J Chorney, C P Venditti, et al.Journal of Inherited Metabolic Disease|October 27, 2004
Congenital cardiomyopathy and pulmonary hypertension: another fatal variant of cytochrome-c oxidase deficiencyC P Venditti, M C Harris, D Huff, et al.Blood Cells, Molecules & Diseases|January 1, 1996
Mutation analysis in hereditary hemochromatosisE Beutler, T Gelbart, C West, et al.Journal of Inherited Metabolic Disease|December 6, 2013
Update on transcobalamin deficiency: clinical presentation, treatment and outcomeY J Trakadis, A Alfares, O A Bodamer, et al.Pageof 2