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Nouvelle Revue Francaise D'Hematologie|July 1, 1975
[Hemoglobin Stanleyville II and mucoviscidosis in an Alsatian family]M L North, P D Darbre, J G Juif, et al.
Prenatal Diagnosis|October 20, 2000
Evaluation of the prenatal diagnosis of limb reduction deficiencies. EUROSCAN Study GroupC Stoll, A Wiesel, A Queisser-Luft, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|February 24, 2019
Mitochondrial and calcium perturbations in rat CNS neurons induce calpain-cleavage of Parkin: Phosphatase inhibition stabilizes pSer65Parkin reducing its calpain-cleavageHu Wang, Fanny Cheung, Anna C Stoll, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|November 1, 1992
[Familial polymorph ventricular extrasystole associated with Pierre Robin syndrome]J R Kieny, C Stoll, G Roul, et al.
Archives Francaises De Pediatrie|May 1, 1978
[A new family with mutation of the structural gene of human ornithine carbamoyltransferase]C Stoll, R Bieth, J Dreyfus, et al.
Journal De Genetique Humaine|March 1, 1976
[Polycystic kidney disease of the newborn in two different sibships]C Stoll, D Willard, P Beauvais, et al.
Genes and Immunity|January 22, 2004
A vulnerability locus to multiple sclerosis maps to 7p15 in a region syntenic to an EAE locus in the ratH Coppin, M-T Ribouchon, B Fontaine, et al.
Journal of Neuroimmunology|April 1, 1994
Tumor necrosis factor polymorphism in multiple sclerosis: no additional association independent of HLAM P Roth, L Nogueira, H Coppin, et al.
Digestive Diseases and Sciences|June 1, 1992
Risk factors for gallstone formation during rapid loss of weightH Yang, G M Petersen, M P Roth, et al.
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