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Molecular Syndromology|December 6, 2011
Unmasking of a Recessive SCARF2 Mutation by a 22q11.12 de novo Deletion in a Patient with Van den Ende-Gupta SyndromeM F Bedeschi, L Colombo, F Mari, et al.
Il Giornale Di Chirurgia|June 10, 2009
A rare case of blunt thoracoabdominal trauma with small bowel perforation from air bagsA Liverani, M Pezzatini, S Conte, et al.
Bone and Mineral|October 1, 1992
Ipriflavone and low doses of estrogens in the prevention of bone mineral loss in climacteriumG B Melis, A M Paoletti, R Bartolini, et al.
Minerva Cardioangiologica|July 1, 1991
[Subrenal coarctation of the aorta. Presentation of a clinical case]S Occhionorelli, M C Taddia, D Romano, et al.
Acta Neurologica Scandinavica|January 18, 2006
Use of levetiracetam in treating epilepsy associated with other medical conditionsC Di Bonaventura, F Mari, J Fattouch, et al.
Clinical Genetics|February 28, 2004
Chromosome 2 deletion encompassing the MAP2 gene in a patient with autism and Rett-like featuresC Pescucci, I Meloni, M Bruttini, et al.
Minerva Cardioangiologica|March 1, 1990
[Isthmic coarctation of the aorta. Description of an anomalous case]F Mascoli, G Anania, T Virgili, et al.
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