Ulf Kristoffersson

Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney disease: linkage to 1q21-q32 and loss of the wild type allele in renal hamartomas.

Bin Tean Teh, Filip Farnebo, Ulf Kristoffersson et al. · The Journal of Clinical Endocrinology & Metabolism · 1996 · 155 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Frequency of RET mutations in long- and short-segment Hirschsprung disease

Marco Seri, Virginia Barone, Alessandra Bolino et al. · Human Mutation · 1997 · 137 citations

Life Sciences, Genetics, Molecular Genetics +16

Segregation analysis of balanced pericentric inversions in pedigree data

Stephanie L. Sherman, L Iselius, P. Gallano et al. · Clinical Genetics · 1986 · 107 citations

Life Sciences, Genetics, Molecular Genetics +11

Marker ring chromosome—A new cytogenetic abnormality characterizing lipogenic tumors?

Sverre Heim, Nils Mandahl, Ulf Kristoffersson et al. · Cancer Genetics and Cytogenetics · 1987 · 84 citations

Life Sciences, Genetics, Oncology +14

Heterogeneity and Low DetectionRate of RET Mutations inHirschsprung Disease

Isabella Ceccherini, Barbara Pasini, Tatiana Tocco et al. · European Journal of Human Genetics · 1994 · 66 citations

Life Sciences, Genetics, Molecular Genetics +15