Cita APA

PRITCHARD-JONES, K., RAHMAN, N., GERRARD, M., VARIEND, D., & KING-UNDERWOOD, L. (2000). Familial Wilms tumour resulting from WT1 mutation: Intronic polymorphism causing artefactual constitutional homozygosity. BMJ Group.

Citación estilo Chicago

PRITCHARD-JONES, K., N. RAHMAN, M. GERRARD, D. VARIEND, y L. KING-UNDERWOOD. Familial Wilms Tumour Resulting From WT1 Mutation: Intronic Polymorphism Causing Artefactual Constitutional Homozygosity. BMJ Group, 2000.

Cita MLA

PRITCHARD-JONES, K., et al. Familial Wilms Tumour Resulting From WT1 Mutation: Intronic Polymorphism Causing Artefactual Constitutional Homozygosity. BMJ Group, 2000.