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A CHILD WITH DOUBLE TRISOMY: 48, XYY, +18FELDING I; KRISTOFFERSSON U.1981; HERIDITAS; ISSN 0018-0661; SWE; DA. 1981; VOL. 95; NO 1; PP. 169-171; BIBL. 2 REF.Article

Partial trisomy 15(q25qter) in two brothersKRISTOFFERSSON, U; BERGWALL, B.Hereditas (Landskrona). 1984, Vol 100, Num 1, pp 7-10, issn 0018-0661Article

FINE NEEDLE ASPIRATION BIOPSY: A USEFUL TOOL IN TUMOR CYTOGENETICS WITH SPECIAL REFERENCE TO MALIGNANT LYMPHOMASKRISTOFFERSSON U; OLSSON H; MARK VENDEL E et al.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 4; NO 1; PP. 53-60; BIBL. 5 REF.Article

The risk of malignant tumours in first-degree relatives of men with early onset prostate cancer : A population-based cohort studyBRATT, O; KRISTOFFERSSON, U; LUNDGREN, R et al.European journal of cancer (1990). 1997, Vol 33, Num 13, pp 2237-2240, issn 0959-8049Article

Relation between occupational exposure to organic solvents and chromosome aberrations in non-Hodgkin's lymphomaBRANDT, L; KRISTOFFERSSON, U; OLSSON, H et al.European journal of haematology. 1989, Vol 42, Num 3, pp 298-302, issn 0902-4441Article

Chromosome analysis of a newly established renal carcinoma cell lineKRISTOFFERSSON, U; YUE-SHENG JIN; LUNDGREN, R et al.Cancer genetics and cytogenetics. 1988, Vol 33, Num 1, pp 133-138, issn 0165-4608Article

Proliferative activity and number of clonal chromosome aberrations in non-Hodgkin's lymphomasBRANDT, L; KRISTOFFERSSON, U; OLSSON, H et al.Scandinavian journal of haematology. 1986, Vol 37, Num 2, pp 106-110, issn 0036-553XArticle

Cytogenetic studies in non-Hodgkin lymphomas ― results from fine-needle aspiration samplesKRISTOFFERSSON, U; OLSSON, H; AKERMAN, M et al.Hereditas (Landskrona). 1985, Vol 103, Num 1, pp 63-76, issn 0018-0661Article

Hypereosinophilic syndrome in a child mosaic for a congenital triplication of the short arm of chromosome 8EGESTEN, A; HÄGERSTRAND, I; KRISTOFFERSSON, U et al.British journal of haematology. 1997, Vol 96, Num 2, pp 369-373, issn 0007-1048Article

Four copies of 8p in a mentally retarded boy with the mosaic karyotype 47,XY,+i(8p)/46,XYKRISTOFFERSSON, U; LAGERGREN, J; HEIM, S et al.Clinical genetics. 1988, Vol 34, Num 3, pp 201-203, issn 0009-9163Article

Hypophyseal tumor and gynecomastia preceding bilateral breast cancer development in a man = Tumeur hypophysqire et gynécomastie précédant un cancer bilatéral du sein chez un hommeOLSSON, H; KRISTOFFERSSON, U; LANDIN-OLSSON, M et al.Cancer. 1984, Vol 53, Num 9, pp 1974-1977, issn 0008-543XArticle

Familial and hereditary prostate cancer in southern Sweden. A population-based case-control studyBRATT, O; KRISTOFFERSSON, U; LUNDGREN, R et al.European journal of cancer (1990). 1999, Vol 35, Num 2, pp 272-277, issn 0959-8049Article

Clinical course of early onset prostate cancer with special reference to family history as a prognostic factorBRATT, O; KRISTOFFERSSON, U; OLSSON, H et al.European urology. 1998, Vol 34, Num 1, pp 19-24, issn 0302-2838Article

Sons of men with prostate cancer : Their attitudes regarding possible inheritance of prostate cancer, screening, and genetic testingBRATT, O; KRISTOFFERSSON, U; LUNDGREN, R et al.Urology (Ridgewood, NJ). 1997, Vol 50, Num 3, pp 360-365, issn 0090-4295Article

No correlation between hyperthermia during pregnancy and Hirschsprung disease in the offspringLARSSON, L. T; OKMIAN, L; KRISTOFFERSSON, U et al.American journal of medical genetics. 1989, Vol 32, Num 2, pp 260-261, issn 0148-7299Article

Contribution to the 18q- syndrome. A patient with del(18) (q22.3qter)FELDING, I; KRISTOFFERSSON, U; SJOSTROM, H et al.Clinical genetics. 1987, Vol 31, Num 4, pp 206-210, issn 0009-9163Article

Novel germline APC mutations in swedish patients with familial adenomatous polyposis and Gardner syndromeNILBERT, M; FERNEBRO, J; KRISTOFFERSSON, U et al.Scandinavian journal of gastroenterology. 2000, Vol 35, Num 11, pp 1200-1203, issn 0036-5521Article

Pseudohypoparathyroidism type I and Albright's hereditary osteodystrophy with a proximal 15q chromosomal deletion in mother and daughterHEDELAND, H; BERNTORP, K; ARHEDEN, K et al.Clinical genetics. 1992, Vol 42, Num 3, pp 129-134, issn 0009-9163Article

Constitutive heterochromatin C-band polymorphism in prostatic cancerLUNDGREN, R; BERGER, R; KRISTOFFERSSON, U et al.Cancer genetics and cytogenetics. 1991, Vol 51, Num 1, pp 57-62, issn 0165-4608, 6 p.Article

Multiple clonal chromosome aberrations in two thymomasKRISTOFFERSSON, U; HEIM, S; MANDAHL, N et al.Cancer genetics and cytogenetics. 1989, Vol 41, Num 1, pp 93-98, issn 0165-4608Article

Differences in human c-band pattern between two european populationsBERGER, R; BERNHEIM, A; KRISTOFFERSSON, U et al.Hereditas (Landskrona). 1983, Vol 99, Num 1, pp 147-149, issn 0018-0661Article

Late appearing 5q―Marker in refractory anemiaHEIM, S; BILLSTROM, R; KRISTOFFERSSON, U et al.Cancer genetics and cytogenetics. 1987, Vol 24, Num 1, pp 159-162, issn 0165-4608Article

Near-haploidy in a case of plasmocytomaKRISTOFFERSSON, U; OLSSON, H; KELLY, D et al.Cancer genetics and cytogenetics. 1986, Vol 19, Num 3-4, pp 239-243, issn 0165-4608Article

Karyotypic patterns in chronic myeloproliferative disorders : report on 74 cases and review of the literatureMERTENS, F; JOHANSSON, B; HEIM, S et al.Leukemia. 1991, Vol 5, Num 3, pp 214-220, issn 0887-6924, 7 p.Article