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Clinical Dysmorphology|April 20, 2001
Inherited duplication of Xq27.2-->qter: phenocopy of infantile Prader-Willi syndromeE J Lammer, D R Punglia, A E Fuchs, et al.
Histopathology|March 4, 1999
Diagnostic markers in paediatric medulloblastoma: a Paediatric Oncology Group StudyR E McLendon, H S Friedman, H E Fuchs, et al.
Andrology|December 15, 2015
Pre-operative risk factors associated with need for vasoepididymostomy at the time of vasectomy reversalM E Fuchs, R E Anderson, K A Ostrowski, et al.
Proteins|October 3, 2013
Specificity of a protein-protein interface: local dynamics direct substrate recognition of effector caspasesJulian E Fuchs, Susanne von Grafenstein, Roland G Huber, et al.
International Journal of Molecular Sciences|June 8, 2017
Conformational Flexibility Differentiates Naturally Occurring Bet v 1 IsoformsSarina Grutsch, Julian E Fuchs, Linda Ahammer, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 15, 1993
Disease severity correlates with position of keratin point mutations in patients with epidermolysis bullosa simplexA Letai, P A Coulombe, M B McCormick, et al.
Nutrition and Cancer|November 24, 2021
Vitamin B12 Supplementation and Vitamin B12 Blood Serum Levels: Evaluation of Effect Modification by Gender and Smoking StatusHannah E Fuchs, Kelli O'Connell, Mengmeng Du, et al.
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