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Results: 1-8 |
Results: 8
The mannose binding lectin gene influences the severity of chronic liver disease in cystic fibrosis
Authors: Gabolde, M Hubert, D Guilloud-Bataille, M Lenaerts, C Feingold, J Besmond, C
Citation: M. Gabolde et al., The mannose binding lectin gene influences the severity of chronic liver disease in cystic fibrosis, J MED GENET, 38(5), 2001, pp. 310-311
A simple approach to the characterization of three common Indian beta-thalassemia mutations by artificially created restriction sites
Authors: Pawar, AR Lu, CY Besmond, C Gorakshakar, AC Colah, RB Mohanty, D Krishnamoorthy, R
Citation: Ar. Pawar et al., A simple approach to the characterization of three common Indian beta-thalassemia mutations by artificially created restriction sites, HEMOGLOBIN, 24(4), 2000, pp. 311-318
Genotyping of the three major allelic variants of the human mannose-binding lectin gene by denaturing gradient gel electrophoresis
Authors: Gabolde, M Muralitharan, S Besmond, C
Citation: M. Gabolde et al., Genotyping of the three major allelic variants of the human mannose-binding lectin gene by denaturing gradient gel electrophoresis, HUM MUTAT, 14(1), 1999, pp. 80-83
Genetic polymorphism of the mannose-binding protein gene in children with sickle cell disease: identification of three new variant alleles and relationship to infections
Authors: Neonato, MG Lu, CY Guilloud-Bataille, M Lapoumeroulie, C Nabeel-Jassim, H Dabit, D Girot, R Krishnamoorthy, R Feingold, J Besmond, C Elion, J
Citation: Mg. Neonato et al., Genetic polymorphism of the mannose-binding protein gene in children with sickle cell disease: identification of three new variant alleles and relationship to infections, EUR J HUM G, 7(6), 1999, pp. 679-686
Human RAGE GLY82SER dimorphism and HLA class II DRB1-DQA1-DQB1 haplotypes in type 1 diabetes
Authors: Prevost, G Fajardy, I Fontaine, P Danze, PM Besmond, C
Citation: G. Prevost et al., Human RAGE GLY82SER dimorphism and HLA class II DRB1-DQA1-DQB1 haplotypes in type 1 diabetes, EUR J IMM, 26(5), 1999, pp. 343-348
Association of variant alleles of mannose binding lectin with severity of pulmonary disease in cystic fibrosis: cohort study
Authors: Gabolde, M Guilloud-Bataille, M Feingold, J Besmond, C
Citation: M. Gabolde et al., Association of variant alleles of mannose binding lectin with severity of pulmonary disease in cystic fibrosis: cohort study, BR MED J, 319(7218), 1999, pp. 1166-1167
Potential of denaturing gradient gel electrophoresis for scanning of beta-thalassemia mutations in India
Authors: Gorakshakar, AC Pawar, AR Nadkarni, AH Lu, CY Mohanty, D Krishnamoorthy, R Besmond, C Colah, RB
Citation: Ac. Gorakshakar et al., Potential of denaturing gradient gel electrophoresis for scanning of beta-thalassemia mutations in India, AM J HEMAT, 61(2), 1999, pp. 120-125
Evaluation of parental mitochondrial inheritance in neonates born after intracytoplasmic sperm injection
Authors: Danan, C Sternberg, D Van Steirteghem, A Cazeneuve, C Duquesnoy, P Besmond, C Goossens, M Lissens, W Amselem, S
Citation: C. Danan et al., Evaluation of parental mitochondrial inheritance in neonates born after intracytoplasmic sperm injection, AM J HU GEN, 65(2), 1999, pp. 463-473
Risultati: 1-8 |