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Human Genetics|August 1, 1987
Linkage relationships and allelic associations of the cystic fibrosis locus and four marker lociJ Schmidtke, M Krawczak, M Schwartz, et al.Human Genetics|May 17, 2001
Increased reproductive success of MHC class II heterozygous males among free-ranging rhesus macaquesU Sauermann, P Nürnberg, F B Bercovitch, et al.Czechoslovak Medicine|January 11, 1990
The rapid molecular genetic diagnosis of cystic fibrosis by polymerase chain reaction: an experience reportM Macek, I Boehm, L Arnold, et al.Human Genetics|September 1, 1990
Frequency of the F508 deletion in the CFTR gene in Turkish cystic fibrosis patientsJ Hundrieser, S Bremer, F Peinemann, et al.Clinical Genetics|January 24, 1998
Detection of 100% of the CFTR mutations in 63 CF families from TyrolM Stuhrmann, T Dörk, M Frühwirth, et al.Human Genetics|September 1, 1990
Frequency of the delta F508 mutation and flanking marker haplotypes at the CF locus from 167 Czech familiesM Macek, V Vavrová, I Böhm, et al.Prenatal Diagnosis|October 1, 1988
Prenatal diagnosis of cystic fibrosis using linked DNA probesM Schwartz, M Super, J Schmidtke, et al.European Journal of Pediatrics|December 1, 1990
Isolated and combined deficiencies of NADH dehydrogenase (complex I) in muscle tissue of children with mitochondrial myopathiesG C Korenke, H A Bentlage, W Ruitenbeek, et al.Annals of Neurology|July 1, 1992
L-2-hydroxyglutaric acidemia: a novel inherited neurometabolic diseaseP G Barth, G F Hoffmann, J Jaeken, et al.Pediatrics|December 1, 1991
Glutaryl-coenzyme A dehydrogenase deficiency: a distinct encephalopathyG F Hoffmann, F K Trefz, P G Barth, et al.Pageof 33