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Clinical Genetics|March 19, 2010
X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findingsF Clauss, N Chassaing, A Smahi, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|February 18, 1980
[Sensibility to insulin in obese children (author's transl)]J M Levy, C Stoll, R Thierry, et al.
Cell and Tissue Banking|July 17, 2004
Validation of bone conversion in osteoconductive and osteoinductive bone substitutesF Soost, S Koch, C Stoll, et al.
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.
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