Two pericentric inversions of human chromosome 11.

Por Simola, K, Karli, P, De La Chapelle, A
Publicado em 1977

Clinical features of nine males with molecularly defined deletions of the Y chromosome long arm.

Por Salo, P, Ignatius, J, Simola, K O, Tahvanainen, E, Kääriäinen, H
Publicado em 1995

Segregation and fertility analysis in an autosomal reciprocal translocation, t(1;8)(q41;q23.1).

Por Vauhkonen, A E, Sankila, E M, Simola, K O, de la Chapelle, A
Publicado em 1985

HRAS1-selected chromosome transfer generates markers that colocalize aniridia- and genitourinary dysplasia-associated translocation breakpoints and the Wilms tumor gene within band...

Por Porteous, D J, Bickmore, W, Christie, S, Boyd, P A, Cranston, G, Fletcher, J M, Gosden, J R, Rout, D, Seawright, A, Simola, K O
Publicado em 1987

Germline Mutations in RASA1 Are Not Found in Patients with Klippel-Trenaunay Syndrome or Capillary Malformation with Limb Overgrowth

Por Revencu, N., Boon, L.M., Dompmartin, A., Rieu, P., Busch, W.L., Dubois, J., Forzano, F., van Hagen, J.M., Halbach, S., Kuechler, A., Lachmeijer, A.M.A., Lähde, J., Russell, L., Simola, K.O.J., Mulliken, J.B., Vikkula, M.
Publicado em 2013