Evidence for “Deleted” or “Silent” gene homozygous at the locus coding for the constant region of the γ3 chain

Por Lefranc, G., Rivat, L., Rivat, C., Loiselet, J., Ropartz, C.
Publicado em 1976

Further refinement of Pendred syndrome locus by homozygosity analysis to a 0.8 cM interval flanked by D7S496 and D7S2425.

Por Mustapha, M, Azar, S T, Moglabey, Y B, Saouda, M, Zeitoun, G, Loiselet, J, Slim, R
Publicado em 1998

Autosomal recessive non-syndromic hearing loss in the Lebanese population: prevalence of the 30delG mutation and report of two novel mutations in the connexin 26 (GJB2) gene

Por Mustapha, M., Salem, N., Delague, V., Chouery, E., Ghassibeh, M., Rai, M., Loiselet, J., Petit, C., Megarbane, A.
Publicado em 2001

Recombination, mutation, or constitutive expression at a Gm locus and familial hypergammaglobulinemia.

Por Lefranc, G, Rivat, L, Salier, J P, van Loghem, E, Aydenian, H, Zalzal, P, Chakhachiro, L, Loiselet, J, Ropartz, C
Publicado em 1977

Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins.

Por Richard, I, Brenguier, L, Dinçer, P, Roudaut, C, Bady, B, Burgunder, J M, Chemaly, R, Garcia, C A, Halaby, G, Jackson, C E, Kurnit, D M, Lefranc, G, Legum, C, Loiselet, J, Merlini, L, Nivelon-Chevallier, A, Ollagnon-Roman, E, Restagno, G, Topaloglu, H, Beckmann, J S
Publicado em 1997