A new TaqI allele at DXS52 frequent in Algeria.

بواسطة Nafa, K, Reghis, A, Benabadji, M, Delpech, M, Kaplan, J C
منشور في 1989

Clinical significance of P46L and R92Q substitutions in the tumour necrosis factor superfamily 1A gene

بواسطة Ravet, N, Rouaghe, S, Dodé, C, Bienvenu, J, Stirnemann, J, Lévy, P, Delpech, M, Grateau, G
منشور في 2006

Unexpected Angelman syndrome molecular defect in a girl displaying clinical features of Prader-Willi syndrome

بواسطة DUPONT, J., LE TESSIER, D., RABINEAU, D., CUISSET, L., VASSEUR, C., JEANPIERRE, M., DELPECH, M., PINTON, F., PONSOT, G., DENAVIT, M.
منشور في 1999

Genotypic diagnosis of familial Mediterranean fever (FMF) using new microsatellite markers: example of two extensive non-Ashkenazi Jewish pedigrees.

بواسطة Dupont, M, Dross, C, Smaoui, N, Nedelec, B, Grateau, G, Clépet, C, Gourdier, I, Koné-Paut, I, Delpech, M, Demaille, J, Touitou, I
منشور في 1997

MEFV-Gene analysis in armenian patients with Familial Mediterranean fever: diagnostic value and unfavorable renal prognosis of the M694V homozygous genotype-genetic and therapeutic...

بواسطة Cazeneuve, C, Sarkisian, T, Pêcheux, C, Dervichian, M, Nédelec, B, Reinert, P, Ayvazyan, A, Kouyoumdjian, J C, Ajrapetyan, H, Delpech, M, Goossens, M, Dodé, C, Grateau, G, Amselem, S
منشور في 1999