Showing results (101-110 of 140) with videos related to

Sort By:
Pageof 14
Journal of Inherited Metabolic Disease|January 1, 1991
Prenatal diagnosis of molybdenum cofactor deficiency by assay of sulphite oxidase activity in chorionic villus samplesJ L Johnson, K V Rajagopalan, J T Lanman, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 1, 2004
A survey of factor prophylaxis in the Canadian haemophilia A populationP Blanchette, G Rivard, S Israels, et al.
The New England Journal of Medicine|June 12, 1975
Nonketotic hyperglycinemia. Glycine accumulation due to absence of glycerine cleavage in brainT L Perry, N Urquhart, J MacLean, et al.
Bone Marrow Transplantation|August 1, 1994
Bone marrow transplantation in Gaucher's disease: effect of mixed chimeric stateK W Chan, L T Wong, D Applegarth, et al.
The American Journal of Gastroenterology|November 1, 1993
Barrett's esophagus in children with cystic fibrosis: not a coincidental associationE Hassall, D M Israel, A G Davidson, et al.
Brain : a Journal of Neurology|January 3, 2001
The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathyP F Chinnery, D T Brown, R M Andrews, et al.
The Journal of Infectious Diseases|January 1, 1993
Pseudomonas aeruginosa colonization of the gastrointestinal tract in patients with cystic fibrosisD P Speert, M E Campbell, A G Davidson, et al.
Pageof 14