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American Journal of Human Genetics|December 1, 1994
Evidence that the Saethre-Chotzen syndrome locus lies between D7S664 and D7S507, by genetic analysis and detection of a microdeletion in a patientA F Lewanda, E D Green, J Weissenbach, et al.Bone Marrow Transplantation|April 19, 2005
The hemochromatosis C282Y allele: a risk factor for hepatic veno-occlusive disease after hematopoietic stem cell transplantationA R Kallianpur, L D Hall, M Yadav, et al.The Journal of Clinical Endocrinology and Metabolism|June 1, 1996
Recurrent mutations in the vasopressin-neurophysin II gene cause autosomal dominant neurohypophyseal diabetes insipidusD R Repaske, M L Summar, M R Krishnamani, et al.Kidney International|February 1, 1996
Angiotensin converting enzyme gene polymorphism: potential silencer motif and impact on progression in IgA nephropathyT E Hunley, B A Julian, J A Phillips, et al.American Journal of Medical Genetics|December 4, 1995
Benzoate therapy and carnitine deficiency in non-ketotic hyperglycinemiaJ L Van Hove, P Kishnani, J Muenzer, et al.Journal of Neurosurgical Sciences|November 1, 2012
Dexamethasone significantly attenuates sub-arachnoid hemorrhage-induced elevation in cerebrospinal fluid citrulline and leukocytesD E Spratt, V K Reddy, A A Choxi, et al.Gene|July 11, 2003
Characterization of genomic structure and polymorphisms in the human carbamyl phosphate synthetase I geneM L Summar, L D Hall, A M Eeds, et al.Pageof 3