Showing results (31-40 of 250) with videos related to
Sort By:
Pageof 25
Current Opinion in Neurology|March 31, 1999
Vestibular and hearing loss in genetic and metabolic disordersP Gasparini, X Estivill, P FortinaHuman Mutation|September 12, 2000
Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexinsR Rabionet, P Gasparini, X EstivillHaematologica|September 8, 1999
The influence of hemochromatosis mutations on iron overload of thalassemia majorF Longo, G Zecchina, L Sbaiz, et al.Blood Cells, Molecules & Diseases|June 22, 2005
Juvenile hemochromatosis due to G320V/Q116X compound heterozygosity of hemojuvelin in an Irish patientF Daraio, E Ryan, F Gleeson, et al.The Journal of Pediatrics|December 25, 2007
Natural history of recessive inheritance of DMT1 mutationsA Iolascon, C Camaschella, D Pospisilova, et al.Blood|November 1, 1975
The relationship between anemia, fecal stercobilinogen, erythrocyte survival, and globin synthesis in heterozygotes for beta-thalassemiaE Gallo, P Pich, G Ricco, et al.The EMBO Journal|April 1, 1984
The beta-globin gene in Sardinian delta beta 0-thalassemia carries a C----T nonsense mutation at codon 39S Guida, B Giglioni, P Comi, et al.Prenatal Diagnosis|October 1, 1988
Circulating 'trophoblast' cells in pregnancy have maternal genetic markersM T Bertero, C Camaschella, A Serra, et al.Human Genetics|June 1, 1994
A unique origin for Sicilian (delta beta) (0)-thalassemia in 33 unrelated families and its rapid diagnostic characterization by PCR analysisG Esposito, M Grosso, E Gottardi, et al.Recenti Progressi in Medicina|October 1, 1989
Hypothalamic pituitary adrenal function in patients with thalassemia majorD Bisbocci, C Camaschella, D Sperone, et al.Pageof 25