Class II-antigen-negative patient and mutant B-cell lines represent at least three, and probably four, distinct genetic defects defined by complementation analysis.

Por Bénichou, B, Strominger, J L
Publicado em 1991

Large deletion of the peroxisomal acyl-CoA oxidase gene in pseudoneonatal adrenoleukodystrophy.

Por Fournier, B, Saudubray, J M, Benichou, B, Lyonnet, S, Munnich, A, Clevers, H, Poll-The, B T
Publicado em 1994

Mutations in the D strand of the human CD4 V1 domain affect CD4 interactions with the human immunodeficiency virus envelope glycoprotein gp120 and HLA class II antigens similarly.

Por Piatier-Tonneau, D, Gastinel, L N, Moussy, G, Bénichou, B, Amblard, F, Vaigot, P, Auffray, C
Publicado em 1991

Mapping of X-linked myxomatous valvular dystrophy to chromosome Xq28.

Por Kyndt, F, Schott, J J, Trochu, J N, Baranger, F, Herbert, O, Scott, V, Fressinaud, E, David, A, Moisan, J P, Bouhour, J B, Le Marec, H, Bénichou, B
Publicado em 1998