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FEBS Letters|January 13, 1997
Expression of receptors for native and chemically modified low-density lipoproteins in brain microvesselsM Lucarelli, M Gennarelli, P Cardelli, et al.Clinical Genetics|November 15, 2005
Pachydermoperiostosis: an updateM Castori, L Sinibaldi, R Mingarelli, et al.American Journal of Medical Genetics|November 1, 1993
Parental origin of chromosome 4p deletion in Wolf-Hirschhorn syndromeB Dallapiccola, P Mandich, E Bellone, et al.American Journal of Medical Genetics|October 1, 1994
Hypoparathyroidism as the major manifestation in two patients with 22q11 deletionsG Scirè, B Dallapiccola, P Iannetti, et al.Journal of Medical Genetics|March 1, 1995
Neonatal spinal muscular atrophy with diaphragmatic paralysis is unlinked to 5q11.2-q13G Novelli, F Capon, L Tamisari, et al.Neuropediatrics|May 7, 2010
Normal cognitive functions in joubert syndromeA Poretti, F Dietrich Alber, F Brancati, et al.Journal of Chromatography|May 28, 1993
Detection by capillary electrophoresis of restriction fragment length polymorphism. Analysis of a polymerase chain reaction-amplified product of the DXS 164 locus in the dystrophin geneD Del Principe, M P Iampieri, D Germani, et al.The American Journal of Cardiology|March 1, 1996
Associated cardiac anomalies in isolated and syndromic patients with tetralogy of FallotB Marino, M C Digilio, S Grazioli, et al.Cell Biochemistry and Function|September 1, 1993
Isolation and cloning by a polymerase chain reaction of a genomic DNA fragment of the human slow skeletal troponin (TNNT1) geneG Novelli, M Gennarelli, F Sangiuolo, et al.Molecular and Cellular Probes|June 1, 1993
A tool for the molecular analysis of an early lethal disease: slide-PCR in spinal muscular atrophy patientsF Capon, S Melchionda, M Gennarelli, et al.Pageof 34