Deletion 14q (q22q23) associated with anophthalmia, absent pituitary, and other abnormalities.

Por Bennett, C P, Betts, D R, Seller, M J
Publicado em 1991

Molecular features of a human rhabdomyosarcoma cell line with spontaneous metastatic progression

Por Scholl, F A, Betts, D R, Niggli, F K, Schäfer, B W
Publicado em 2000

Cytogenetic abnormalities in Langerhans cell histiocytosis.

Por Betts, D. R., Leibundgut, K. E., Feldges, A., Plüss, H. J., Niggli, F. K.
Publicado em 1998

Duplication of 17q11.2 and Features of Albright Hereditary Osteodystrophy Secondary to Methylation Defects within the GNAS Cluster: Coincidence or Causal?

Por White, M., Conroy, J., Bullman, H., Lever, M., Daly, E., Betts, D. R., Cody, D., Crolla, John A., Lynch, S. A.
Publicado em 2013

Prognostic impact of chromosomal aberrations in Ewing tumours

Por Hattinger, C M, Pötschger, U, Tarkkanen, M, Squire, J, Zielenska, M, Kiuru-Kuhlefelt, S, Kager, L, Thorner, P, Knuutila, S, Niggli, F K, Ambros, P F, Gadner, H, Betts, D R
Publicado em 2002