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Clinical Genetics|September 1, 1992
Pseudohypoparathyroidism type I and Albright's hereditary osteodystrophy with a proximal 15q chromosomal deletion in mother and daughterH Hedeland, K Berntorp, K Arheden, et al.Clinical Genetics|September 1, 1988
Four copies of 8p in a mentally retarded boy with the mosaic karyotype 47,XY, + i(8p)/46,XYU Kristoffersson, J Lagergren, S Heim, et al.Urology|September 25, 1997
Sons of men with prostate cancer: their attitudes regarding possible inheritance of prostate cancer, screening, and genetic testingO Bratt, U Kristoffersson, R Lundgren, et al.European Journal of Cancer (Oxford, England : 1990)|February 21, 1998
The risk of malignant tumours in first-degree relatives of men with early onset prostate cancer: a population-based cohort studyO Bratt, U Kristoffersson, R Lundgren, et al.Human Mutation|August 14, 1999
A methylation PCR approach for detection of fragile X syndromeI Panagopoulos, C Lassen, U Kristoffersson, et al.European Journal of Cancer (Oxford, England : 1990)|August 17, 1999
Familial and hereditary prostate cancer in southern Sweden. A population-based case-control studyO Bratt, U Kristoffersson, R Lundgren, et al.European Urology|July 24, 1998
Clinical course of early onset prostate cancer with special reference to family history as a prognostic factorO Bratt, U Kristoffersson, H Olsson, et al.Clinical Genetics|April 1, 1987
Contribution to the 18q- syndrome. A patient with del(18) (q22.3qter)I Felding, U Kristoffersson, H Sjöström, et al.Annals of Oncology : Official Journal of the European Society for Medical Oncology|July 29, 2004
External quality assessment for mutation detection in the BRCA1 and BRCA2 genes: EMQN's experience of 3 yearsC R Mueller, U Kristoffersson, D Stoppa-LyonnetEuropean Journal of Neurology|October 27, 2015
Familial aggregation of stroke amongst young patients in Lund Stroke RegisterA Ilinca, U Kristoffersson, M Soller, et al.Pageof 11