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Journal of Nephrology|May 28, 2003
Type-IV collagen related diseasesChiara Pescucci, Ilaria Longo, Mirella Bruttini, et al.
Journal of Cellular Physiology|February 4, 2005
Non-syndromic X-linked mental retardation: from a molecular to a clinical point of viewA Renieri, C Pescucci, I Longo, et al.
Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics|April 20, 2004
Saturation and electron-beam lifetime in a storage ring free-electron laserR Bartolini, G Dattoli, L Giannessi, et al.
Brain & Development|May 12, 2009
Leukoencephalopathy in 21-beta hydroxylase deficiency: report of a familyCarmen Gaudiano, Alessandro Malandrini, Marzia Pollazzon, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|November 4, 2005
[Clinical and genetic features of the Alport 'syndromes']C Pescucci, I Longo, F Mari, et al.
Journal of Molecular Medicine (Berlin, Germany)|May 17, 2003
Rett syndrome: the complex nature of a monogenic diseaseAlessandra Renieri, Ilaria Meloni, Ilaria Longo, et al.
International Journal of Radiation Oncology, Biology, Physics|May 1, 1997
A simple method to stabilize the prostate during transperineal prostate brachytherapyM Dattoli, K Waller
American Journal of Medical Genetics. Part A|March 14, 2007
Clinical and molecular characterization of a patient with a 2q31.2-32.3 deletion identified by array-CGHMaria Antonietta Mencarelli, Rossella Caselli, Chiara Pescucci, et al.
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