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Results: 1-7 |
Results: 7
Associated malformations in cases with oral clefts
Authors: Stoll, C Alembik, Y Dott, B Roth, MP
Citation: C. Stoll et al., Associated malformations in cases with oral clefts, CLEF PAL-CR, 37(1), 2000, pp. 41-47
Genetic markers of immunoglobulins and diabetes mellitus in the multiracial population of New Caledonia
Authors: Dugoujon, JM Guitard, E Senegas, MT Roth, MP Sanchez, A Barny, S Simon, D Papoz, L
Citation: Jm. Dugoujon et al., Genetic markers of immunoglobulins and diabetes mellitus in the multiracial population of New Caledonia, DIABET RE C, 47(3), 2000, pp. 209-215
Diagnosis and management of haemochromatosis since the discovery of the HFE gene: A European experience
Authors: Robson, KJH Merryweather-Clark, AT Pointon, JJ Shearman, JD Halsall, DJ Kelly, A Cox, TM Rosenberg, WM Howell, M Eccles, D Patch, C Fowler, AV Wallace, DF Camaschella, C Roetto, A Zecchina, G De Gobbi, M Gasparini, P Cadet, E Vandwalle, JL Capron, D Rochette, J Borot, N Demangel, C Dery, R Vinel, JP Pascal, JP Coppin, H Roth, MP
Citation: Kjh. Robson et al., Diagnosis and management of haemochromatosis since the discovery of the HFE gene: A European experience, BR J HAEM, 108(1), 2000, pp. 31-39
Evaluation of prenatal diagnosis of cleft lip/palate by foetal ultrasonographic examination
Authors: Stoll, C Dott, B Alembik, Y Roth, MP
Citation: C. Stoll et al., Evaluation of prenatal diagnosis of cleft lip/palate by foetal ultrasonographic examination, ANN GENET, 43(1), 2000, pp. 11-14
Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results
Authors: Merryweather-Clarke, AT Pointon, JJ Shearman, JD Robson, KJH Jouanolle, AM Mosser, A David, V Le Gall, JY Halsall, DJ Elsey, TS Kelly, A Cox, TM Clare, M Bomford, A Vandwalle, JL Rochette, J Borot, N Coppin, H Roth, MP Ryan, E Crowe, J Totaro, A Gasparini, P Roetto, A Gamaschella, C Darke, C Wallace, DF Saeb-Parsy, K Dooley, JS Worwood, M Walker, AP
Citation: At. Merryweather-clarke et al., Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results, NAT GENET, 23(3), 1999, pp. 271-271
A genome-wide search identifies two susceptibility loci for experimental autoimmune encephalomyelitis on rat chromosomes 4 and 10
Authors: Roth, MP Viratelle, C Dolbois, L Delverdier, M Borot, N Pelletier, L Druet, P Clanet, M Coppin, H
Citation: Mp. Roth et al., A genome-wide search identifies two susceptibility loci for experimental autoimmune encephalomyelitis on rat chromosomes 4 and 10, J IMMUNOL, 162(4), 1999, pp. 1917-1922
Parental consanguinity as a cause for increased incidence of births defects in a study of 238,942 consecutive births
Authors: Stoll, C Alembik, Y Roth, MP Dott, B
Citation: C. Stoll et al., Parental consanguinity as a cause for increased incidence of births defects in a study of 238,942 consecutive births, ANN GENET, 42(3), 1999, pp. 133-139
Risultati: 1-7 |