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International Journal of Cardiology|February 1, 1985
Genetic heterogeneity of hypertrophic cardiomyopathyA Branzi, G Romeo, S Specchia, et al.Human Genetics|May 1, 1992
Deletion delta F508 and haplotype analysis of CFTR gene region in Slovak CF patientsL Kádasi, J Gécz, J Matúsek, et al.Human Molecular Genetics|November 1, 1995
Interstitial deletion of the endothelin-B receptor gene in the spotting lethal (sl) ratI Ceccherini, A L Zhang, I Matera, et al.Annals of Human Genetics|January 31, 2006
Haplotypes of the human RET proto-oncogene associated with Hirschsprung disease in the Italian population derive from a single ancestral combination of allelesF Lantieri, P Griseri, F Puppo, et al.Calcified Tissue International|October 21, 2003
Association analysis of bone mineral density and single nucleotide polymorphisms in two candidate genes on chromosome 1p36L D Spotila, H Rodriguez, M Koch, et al.British Journal of Haematology|December 23, 2003
Association of T-786C eNOS gene polymorphism with increased susceptibility to acute chest syndrome in females with sickle cell diseaseK Sharan, S Surrey, S Ballas, et al.European Journal of Human Genetics : EJHG|September 12, 2000
A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung diseaseP Griseri, M Sancandi, G Patrone, et al.Bratislavske Lekarske Listy|March 1, 1992
[The delta F508 mutation which causes cystic fibrosis and its association with closely linked DNA polymorphisms in the Slovak population]L Kádasi, J Gécz, A Puliti, et al.Kidney International|August 1, 1995
Gender-dependent disease severity in autosomal polycystic kidney disease of ratsN Gretz, I Ceccherini, B Kränzlin, et al.Journal of Medical Genetics|October 1, 1991
Silent mutations in the phenylalanine hydroxylase gene as an aid to the diagnosis of phenylketonuriaL Kalaydjieva, B Dworniczak, C Aulehla-Scholz, et al.Pageof 8