Showing results (131-140 of 334) with videos related to
Sort By:
Pageof 34
American Journal of Medical Genetics|September 20, 2000
Heterotaxy with left atrial isomerism in a patient with deletion 18pM C Digilio, B Marino, A Giannotti, et al.Biochemical and Biophysical Research Communications|July 16, 1985
Increased rate of superoxide ion generation in Fanconi anemia erythrocytesM Scarpa, A Rigo, F Momo, et al.The Journal of Clinical Investigation|March 1, 1994
Defective respiratory capacity and mitochondrial protein synthesis in transformant cybrids harboring the tRNA(Leu(UUR)) mutation associated with maternally inherited myopathy and cardiomyopathyC Mariotti, V Tiranti, F Carrara, et al.Teratology|April 25, 2000
Familial recurrence of nonsyndromic interrupted aortic arch and truncus arteriosus with atrioventricular canalM C Digilio, B Marino, A M Musolino, et al.Genetic Testing|May 5, 2001
A single strand conformation polymorphism-based carrier test for spinal muscular atrophyS Semprini, A Tacconelli, F Capon, et al.Prenatal Diagnosis|August 1, 1993
On the parental origin of the X's in a prenatally diagnosed 49,XXXXX syndromeG Martini, G Carillo, F Catizone, et al.Journal of Medical Genetics|December 1, 1984
A live infant with trisomy 14 mosaicism and nuclear abnormalities of the neutrophilsB Dallapiccola, G Ferranti, A Giannotti, et al.Journal of Medical Genetics|August 1, 1980
Segregation of an X ring chromosome in two generationsB Dallapiccola, L Bruni, B Boscherini, et al.The American Journal of Cardiology|June 15, 1996
Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresiaM C Digilio, B Marino, S Grazioli, et al.Prenatal Diagnosis|June 1, 1994
First-trimester prenatal diagnosis of spinal muscular atrophy using microsatellite markersS Lo Cicero, F Capon, S Melchionda, et al.Pageof 34