Factor IXBasel: a Swiss family with severe haemophilia B having a point mutation in EGF type B domain.

Por Alkan, M, Rodriguez Ponte, M, Malik, N J, Hofmann, S, Bösch-Al Jadooa, N, Müller, H, Bühler, E M
Publicado em 1991

Paternal origin of the de novo deleted chromosome 4 in Wolf-Hirschhorn syndrome.

Por Tupler, R, Bortotto, L, Bühler, E M, Alkan, M, Malik, N J, Bösch-Al Jadooa, N, Memo, L, Maraschio, P
Publicado em 1992