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Ulf Kristoffersson

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Niclas Hagen; Maria Hedlund; Susanne Lundin; Shai Mulinari; Ulf Kristoffersson
Genetics and democracy-what is the issue?
Susanne Magnusson; David Gisselsson; Ulf Kristoffersson; Thomas Wiebe; Ake Borg; Håkan Olsson
Prevalence of germline TP53 mutations and history of Li-Fraumeni syndrome in families with childhood adrenocortical tumors, choroid plexus tumors, and rhabdomyosarcoma: a population-based survey.
Maria Hedlund; Niclas Hagen; Ulf Kristoffersson
Editorial: genetics and democracy.

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All Publications

2013: Niclas Hagen; Maria Hedlund; Susanne Lundin; Shai Mulinari; Ulf Kristoffersson
Genetics and democracy-what is the issue?
Journal of community genetics 2013;4(2):181-8.
2012: Susanne Magnusson; David Gisselsson; Ulf Kristoffersson; Thomas Wiebe; Ake Borg; Håkan Olsson
Prevalence of germline TP53 mutations and history of Li-Fraumeni syndrome in families with childhood adrenocortical tumors, choroid plexus tumors, and rhabdomyosarcoma: a population-based survey.
Pediatric blood & cancer 2012;59(5):846-53.
2012: Maria Hedlund; Niclas Hagen; Ulf Kristoffersson
Editorial: genetics and democracy.
Journal of community genetics 2012;3(2):57-9.
2012: Susanne Magnusson; Helena Jernström; Ulf Kristoffersson; Thomas Wiebe; Håkan Olsson
Increased incidence of childhood, prostate and breast cancers in relatives of childhood cancer patients.
Familial cancer 2012;11(1):145-55.
2011: Mette Gilling; Karen Friis Henriksen; Vera M Kalscheuer; Ulf Kristoffersson; Allan Lind-Thomsen; Yuan Mang; Morten Møller; Mads Bak; Merete Bugge; Zeynep Tümer; Reinhard Ullmann; Niels Tommerup
Biparental inheritance of chromosomal abnormalities in male twins with non-syndromic mental retardation.
European journal of medical genetics 2011;54(4):e383-8.
2011: Frauke Becker; Carla G van El; Dolores Ibarreta; Eleni Zika; Stuart Hogarth; Pascal Borry; Anne Cambon-Thomsen; Jean-Jacques Cassiman; Gerry Evers-Kiebooms; Shirley Hodgson; A Cécile J W Janssens; Helena Kaariainen; Michael Krawczak; Ulf Kristoffersson; Jan Lubinski; Christine Patch; Victor B Penchaszadeh; Andrew Read; Wolf Rogowski; Jorge Sequeiros; Lisbeth Tranebjaerg; Irene van Langen; Helen Wallace; Ron Zimmern; Jörg Schmidtke; Martina C Cornel
Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities. Background Document to the ESHG recommendations on genetic testing and common disorders.
European journal of human genetics : EJHG 2011;19 Suppl 1():S6-44.
2010: P Javaher; E Nyoungui; Helena Kääriäinen; Ulf Kristoffersson; Irmgard Nippert; Jorge Sequeiros; Jörg Schmidtke
Genetic screening in Europe.
Public health genomics 2010;13(7-8):524-37.
2009: Caroline M Benjamin; Elizabeth N Anionwu; Ulf Kristoffersson; Leo P ten Kate; Anne Marie C Plass; Irmgard Nippert; Claire Julian-Reynier; Hilary J Harris; Joerg Schmidtke; Kirsty Challen; Jean Marc Calefato; Christine Waterman; Eileen Powell; Rodney Harris
Educational priorities and current involvement in genetic practice: a survey of midwives in the Netherlands, UK and Sweden.
Midwifery 2009;25(5):483-99.
2008: Elina Rantanen; Marja Hietala; Ulf Kristoffersson; Irmgard Nippert; Jörg Schmidtke; Jorge Sequeiros; Helena Kääriäinen
Regulations and practices of genetic counselling in 38 European countries: the perspective of national representatives.
European journal of human genetics : EJHG 2008;16(10):1208-16.
2008: Håkan Lövkvist; Jan Gustav Smith; Holger Luthman; Peter Höglund; Bo Norrving; Ulf Kristoffersson; Ann-Cathrin Jönsson; Arne G Lindgren
Ischaemic stroke in hypertensive patients is associated with variations in the PDE4D genome region.
European journal of human genetics : EJHG 2008;16(9):1117-25.
2008: Ulf Kristoffersson
Regulatory issues for genetic testing in clinical practice.
Molecular biotechnology 2008;40(1):113-7.
2008: Elina Rantanen; Marja Hietala; Ulf Kristoffersson; Irmgard Nippert; Jörg Schmidtke; Jorge Sequeiros; Helena Kääriäinen
What is ideal genetic counselling? A survey of current international guidelines.
European journal of human genetics : EJHG 2008;16(4):445-52.
2008: Claire Julian-Reynier; Irmgard Nippert; Jean-Marc Calefato; Hilary Harris; Ulf Kristoffersson; Jörg Schmidtke; Leo P ten Kate; Elizabeth Anionwu; Caroline Benjamin; Kirsty Challen; Anne-Marie Plass; Rodney Harris
Genetics in clinical practice: general practitioners' educational priorities in European countries.
Genetics in medicine : official journal of the American College of Medical Genetics 2008;10(2):107-13.
2008: Jean-Marc Calefato; Irmgard Nippert; Hilary J Harris; Ulf Kristoffersson; Jörg Schmidtke; Leo P ten Kate; Elizabeth Anionwu; Caroline Benjamin; Kirsty Challen; Anne-Marie Plass; Rodney Harris; Claire Julian-Reynier
Assessing educational priorities in genetics for general practitioners and specialists in five countries: factor structure of the Genetic-Educational Priorities (Gen-EP) scale.
Genetics in medicine : official journal of the American College of Medical Genetics 2008;10(2):99-106.
2008: Mef Nilbert; Ulf Kristoffersson; Mats Ericsson; Oskar Johannsson; Eva Rambech; Peter Mangell
Broad phenotypic spectrum in familial adenomatous polyposis; from early onset and severe phenotypes to late onset of attenuated polyposis with the first manifestation at age 72.
BMC medical genetics 2008;9():101.
2008: Susanne Magnusson; Ake Borg; Ulf Kristoffersson; Mef Nilbert; Thomas Wiebe; Håkan Olsson
Higher occurrence of childhood cancer in families with germline mutations in BRCA2, MMR and CDKN2A genes.
Familial cancer 2008;7(4):331-7.
2008: Poupak Javaher; Helena Kaariainen; Ulf Kristoffersson; Irmgard Nippert; Jorge Sequeiros; Ron Zimmern; Jörg Schmidtke
EuroGentest: DNA-based testing for heritable disorders in Europe.
Community genetics 2008;11(2):75-120.
2007: Ros J Hastings; Simona Cavani; Franca Dagna Bricarelli; Philippos C Patsalis; Ulf Kristoffersson
Cytogenetic Guidelines and Quality Assurance: a common European framework for quality assessment for constitutional and acquired cytogenetic investigations.
European journal of human genetics : EJHG 2007;15(5):525-7.
2007: Margaret M McGovern; Rob Elles; Isabella Beretta; Martin J Somerville; Gerald Hoefler; Mauri Keinanen; David Barton; Nancy Carson; Elisabeth Dequeker; Radim Brdicka; Alena Blazkova; Ségolène Aymé; Birgit Schnieders; Clemens R Muller; Vibeke Dalen; Armando Albert Martinez; Ulf Kristoffersson; Meral Ozguc; Hansjakob Mueller; Joe Boone; Ira M Lubin; Jorge Sequeiros; Domenica Taruscio; Bob Williamson; Lynn Mainland; Hiroshi Yoshikura; Elettra Ronchi
Report of an international survey of molecular genetic testing laboratories.
Community genetics 2007;10(3):123-31.
2006: P Gustavsson; Jacqueline Schoumans; Johan Staaf; Göran Jönsson; F Carlsson; Ulf Kristoffersson; Ake Borg; Magnus Nordenskjöld; N Dahl
Hemizygosity for chromosome 2q14.2-q22.1 spanning the GLI2 and PROC genes associated with growth hormone deficiency, polydactyly, deep vein thrombosis and urogenital abnormalities.
Clinical genetics 2006;69(5):441-3.
2006: Susanne Malander; Eva Rambech; Ulf Kristoffersson; Britta Halvarsson; Mona Ridderheim; Ake Borg; Mef Nilbert
The contribution of the hereditary nonpolyposis colorectal cancer syndrome to the development of ovarian cancer.
Gynecologic oncology 2006;101(2):238-43.
2006: Karin Henriksson; Ulf Kristoffersson
Education in medical genetics for non-genetic health care providers in Sweden.
Community genetics 2006;9(4):240-5.
2005: Ulf Kristoffersson; Jan Wahlström; Niels Lynöe
[New discoveries about the fragile X syndrome complicate genetic counseling. More symptoms than earlier known caused by the disease gene].
Läkartidningen 2005;102(44):3232-4, 3236.
2005: Kirsty Challen; Hilary J Harris; Claire Julian-Reynier; Leo P Ten Kate; Ulf Kristoffersson; Irmgard Nippert; Jörg Schmidtke; Caroline Benjamin; Rodney Harris
Genetic education and nongenetic health professionals: educational providers and curricula in Europe.
Genetics in medicine : official journal of the American College of Medical Genetics 2005;7(5):302-10.
2005: Ulf Kristoffersson
[New knowledge of inheritance and heredity and new aspects of heart disease].
Läkartidningen 2005;102(11):826-7.
2005: Arne Lindgren; Håkan Lovkvist; Bjorn Hallstrom; Peter Hoglund; Ann-Cathrin Jonsson; Ulf Kristoffersson; Holger Luthman; Bjorn Petersen; Bo Norrving
Prevalence of stroke and vascular risk factors among first-degree relatives of stroke patients and control subjects. A prospective consecutive study.
Cerebrovascular diseases (Basel, Switzerland) 2005;20(5):381-7.
2004: Susanne Malander; Mona Ridderheim; Anna Måsbäck; Niklas Loman; Ulf Kristoffersson; Håkan Olsson; Mef Nilbert; Ake Borg
One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations: results of a prospective study in Southern Sweden.
European journal of cancer (Oxford, England : 1990) 2004;40(3):422-8.
2004: Karin Henriksson; Håkan Olsson; Ulf Kristoffersson
The need for oncogenetic counselling. Ten years' experience of a regional oncogenetic clinic.
Acta oncologica (Stockholm, Sweden) 2004;43(7):637-49.
2004: Ulf Kristoffersson
Regulation of genetic testing in clinical practice.
Methods in molecular medicine 2004;92():369-75.
2003: Béatrice Godard; Helena Kääriäinen; Ulf Kristoffersson; Lisbeth Tranebjaerg; Domenico A Coviello; Ségolène Aymé
Provision of genetic services in Europe: current practices and issues.
European journal of human genetics : EJHG 2003;11 Suppl 2():S13-48.
2003: Ulf Kristoffersson; Tore Nilstun
[An ethical dilemma: pharmacogenetic tests can yield unwanted information].
Läkartidningen 2003;100(25):2241-2.
2001: Niklas Loman; Oskar T Johannsson; Ulf Kristoffersson; Håkan Olsson; Ake Borg
Family history of breast and ovarian cancers and BRCA1 and BRCA2 mutations in a population-based series of early-onset breast cancer.
Journal of the National Cancer Institute 2001;93(16):1215-23.
2001: Jorge Saraiva; E Anionwu; M Belo; T Jenkins; Ulf Kristoffersson; I Marques; HG Santos; J Sequeiros; S A Simpson; D Wertz; Carolino Monteiro
Issues in human GenEthics.
Genetics in medicine : official journal of the American College of Medical Genetics 2001;3(3):218-9.
2001: Johan Vallon-Christersson; Charmagne Cayanan; Karin Haraldsson; Niklas Loman; Jon Thor Bergthorsson; Karen Brøndum-Nielsen; A M Gerdes; Pål Møller; Ulf Kristoffersson; Håkan Olsson; Ake Borg; Alvaro Monteiro
Functional analysis of BRCA1 C-terminal missense mutations identified in breast and ovarian cancer families.
Human molecular genetics 2001;10(4):353-60.
2001: Christian Olesen; C Hansen; Eske Bendsen; Anne Grete Byskov; E Schwinger; I Lopez-Pajares; Peter Koch Jensen; Ulf Kristoffersson; R Schubert; E Van Assche; J Wahlstroem; James Lespinasse; Niels Tommerup
Identification of human candidate genes for male infertility by digital differential display.
Molecular human reproduction 2001;7(1):11-20.
2000: Ulf Kristoffersson
[Will genetics make a revolution in health care? Skepticism concerning the exaggerated expectations].
Läkartidningen 2000;97(47):5499-501.
2000: Mef Nilbert; Josefin Fernebro; Ulf Kristoffersson
Novel germline APC mutations in Swedish patients with familial adenomatous polyposis and Gardner syndrome.
Scandinavian journal of gastroenterology 2000;35(11):1200-3.
2000: Merete Bugge; Gert Bruun-Petersen; Karen Brøndum-Nielsen; UK Friedrich; J Hansen; G Jensen; Peter Koch Jensen; Ulf Kristoffersson; Claes Lundsteen; Erik Niebuhr; K R Rasmussen; Kirsten Rasmussen; Niels Tommerup
Disease associated balanced chromosome rearrangements: a resource for large scale genotype-phenotype delineation in man.
Journal of medical genetics 2000;37(11):858-65.
2000: Ulf Kristoffersson
The challenge of validating genetic testing.
Community genetics 2000;3(4):170-4.
2000: Ola Bratt; J E Damber; Monica Emanuelsson; Ulf Kristoffersson; Rolf Lundgren; Håkan Olsson; Henrik Grönberg
Risk perception, screening practice and interest in genetic testing among unaffected men in families with hereditary prostate cancer.
European journal of cancer (Oxford, England : 1990) 2000;36(2):235-41.
1999: Maria Planck; Anjila Koul; Eva Fernebro; Ake Borg; Ulf Kristoffersson; Håkan Olsson; E Wenngren; Peter Mangell; Mef Nilbert
hMLH1, hMSH2 and hMSH6 mutations in hereditary non-polyposis colorectal cancer families from southern Sweden.
International journal of cancer. Journal international du cancer 1999;83(2):197-202.
1999: Ola Bratt; A Borg; Ulf Kristoffersson; Rolf Lundgren; Q X Zhang; Håkan Olsson
CAG repeat length in the androgen receptor gene is related to age at diagnosis of prostate cancer and response to endocrine therapy, but not to prostate cancer risk.
British journal of cancer 1999;81(4):672-6.
1999: Oskar T Johannsson; Niklas Loman; Torgil R Möller; Ulf Kristoffersson; Ake Borg; Håkan Olsson
Incidence of malignant tumours in relatives of BRCA1 and BRCA2 germline mutation carriers.
European journal of cancer (Oxford, England : 1990) 1999;35(8):1248-57.
1999: Mats Jerkeman; Bertil Johansson; Måns Akerman; Eva Cavallin-Ståhl; Ulf Kristoffersson; Felix Mitelman
Prognostic implications of cytogenetic aberrations in diffuse large B-cell lymphomas.
European journal of haematology 1999;62(3):184-90.
1999: Ola Bratt; Ulf Kristoffersson; Rolf Lundgren; Håkan Olsson
Familial and hereditary prostate cancer in southern Sweden. A population-based case-control study.
European journal of cancer (Oxford, England : 1990) 1999;35(2):272-7.
1999: Ioannis Panagopoulos; Carin Lassen; Ulf Kristoffersson; Pierre Aman
A methylation PCR approach for detection of fragile X syndrome.
Human mutation 1999;14(1):71-9.
1999: Ioannis Panagopoulos; Carin Lassen; Ulf Kristoffersson; Pierre Aman
A novel PCR-based approach for the detection of the Huntington disease associated trinucleotide repeat expansion.
Human mutation 1999;13(3):232-6.
1998: Ola Bratt; P A Abrahamsson; Rolf Lundgren; Håkan Olsson; Ulf Kristoffersson
[Research progress on hereditary prostatic cancer. Families at risk should be surveyed and screening should be offered].
Läkartidningen 1998;95(14):1494-6.
1998: P Andreasson; Bertil Johansson; K Arheden; Ulf Kristoffersson; Måns Akerman; Felix Mitelman; Mattias Höglund
Genomic amplification of CCND2 is rare in non-Hodgkin lymphomas.
Cancer genetics and cytogenetics 1998;102(1):81-2.
1998: Ola Bratt; Ulf Kristoffersson; Håkan Olsson; Rolf Lundgren
Clinical course of early onset prostate cancer with special reference to family history as a prognostic factor.
European urology 1998;34(1):19-24.
1997: Ola Bratt; Ulf Kristoffersson; Rolf Lundgren; Håkan Olsson
The risk of malignant tumours in first-degree relatives of men with early onset prostate cancer: a population-based cohort study.
European journal of cancer (Oxford, England : 1990) 1997;33(13):2237-40.
1997: Ola Bratt; Ulf Kristoffersson; Rolf Lundgren; Håkan Olsson
Sons of men with prostate cancer: their attitudes regarding possible inheritance of prostate cancer, screening, and genetic testing.
Urology 1997;50(3):360-5.
1997: Bertil Johansson; Rolf Billström; Ulf Kristoffersson; Måns Akerman; Stanislaw Garwicz; Tomas Ahlgren; Claes Malm; Felix Mitelman
Deletion of chromosome arm 3p in hematologic malignancies.
Leukemia 1997;11(8):1207-13.
1997: S Håkansson; Oskar T Johannsson; Ulla Johansson; Gunilla Sellberg; Niklas Loman; A M Gerdes; Erik Holmberg; Niklas Dahl; Nikos Pandis; Ulf Kristoffersson; Håkan Olsson; Ake Borg
Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer.
American journal of human genetics 1997;60(5):1068-78.
1997: Arne Egesten; I Hägerstrand; Ulf Kristoffersson; Stanislaw Garwicz
Hypereosinophilic syndrome in a child mosaic for a congenital triplication of the short arm of chromosome 8.
British journal of haematology 1997;96(2):369-73.
1997: Ulf Kristoffersson
Genetic services in Sweden.
European journal of human genetics : EJHG 1997;5 Suppl 2():169-73.
1996: Ioannis Panagopoulos; Nikos Pandis; S Thelin; C Petersson; Fredrik Mertens; Ake Borg; Ulf Kristoffersson; Felix Mitelman; Pierre Aman
The FHIT and PTPRG genes are deleted in benign proliferative breast disease associated with familial breast cancer and cytogenetic rearrangements of chromosome band 3p14.
Cancer research 1996;56(21):4871-5.
1995: Katarina Hanséus; L M Lundberg; Gudrun Björkhem; K Dahlbäck; I Hägerstrand; Ulf Kristoffersson
Clinical and immunohistochemical findings in a case of neonatal Marfan syndrome.
Acta paediatrica (Oslo, Norway : 1992) 1995;84(11):1329-32.
1993: Thoas Fioretos; Per-Gunnar Nilsson; Pierre Aman; Sverre Heim; Ulf Kristoffersson; Claes Malm; Bengt Simonsson; Ingemar Turesson; Felix Mitelman
Clinical impact of breakpoint position within M-bcr in chronic myeloid leukemia.
Leukemia 1993;7(8):1225-31.
1993: Håkan Olsson; H Andersson; O Johansson; T R Möller; Ulf Kristoffersson; E Wenngren
Population-based cohort investigations of the risk for malignant tumors in first-degree relatives and wives of men with breast cancer.
Cancer 1993;71(4):1273-8.
1991: Fredrik Mertens; B Sallerfors; Sverre Heim; Bertil Johansson; Ulf Kristoffersson; Claes Malm; Felix Mitelman
Trisomy 13 as a primary chromosome aberration in acute leukemia.
Cancer genetics and cytogenetics 1991;56(1):39-44.
1991: Bertil Johansson; Fredrik Mertens; Sverre Heim; Ulf Kristoffersson; Felix Mitelman
Cytogenetics of secondary myelodysplasia (sMDS) and acute nonlymphocytic leukemia (sANLL).
European journal of haematology 1991;47(1):17-27.
1991: Fredrik Mertens; Bertil Johansson; Sverre Heim; Ulf Kristoffersson; Felix Mitelman
Karyotypic patterns in chronic myeloproliferative disorders: report on 74 cases and review of the literature.
Leukemia 1991;5(3):214-20.
1991: Rolf Lundgren; R Berger; Ulf Kristoffersson
Constitutive heterochromatin C-band polymorphism in prostatic cancer.
Cancer genetics and cytogenetics 1991;51(1):57-62.
1990: Bertil Johansson; Fredrik Mertens; Sverre Heim; Ulf Kristoffersson; Nils Mandahl; Per-Gunnar Nilsson; Felix Mitelman
Cytogenetic findings in acute megakaryoblastic leukemia (ANLL-M7).
Cancer genetics and cytogenetics 1990;48(1):119-23.
1990: Bertil Johansson; Fredrik Mertens; Thoas Fioretos; Sverre Heim; Ulf Kristoffersson; Nils Mandahl; C R Bartram; Felix Mitelman
Remarkably long survival of a patient with Ph1-positive chronic myeloid leukemia and 5' bcr rearrangement.
Leukemia 1990;4(6):448-9.
1990: Janusz Limon; Rolf Lundgren; Peter Elfving; Sverre Heim; Ulf Kristoffersson; Nils Mandahl; Felix Mitelman
An improved technique for short-term culturing of human prostatic adenocarcinoma tissue for cytogenetic analysis.
Cancer genetics and cytogenetics 1990;46(2):191-9.
1990: Ulf Kristoffersson; Sverre Heim; A Johnsson; Nils Mandahl; Håkan Olsson; Måns Akerman; Felix Mitelman
Deletion of 14q in non-Hodgkin's lymphoma.
European journal of haematology 1990;44(4):261-4.
1990: Sverre Heim; A N Békàssy; Stanislaw Garwicz; J Heldrup; Ulf Kristoffersson; Nils Mandahl; Thomas Wiebe; Felix Mitelman
Bone marrow karyotypes in 94 children with acute leukemia.
European journal of haematology 1990;44(4):227-33.
1990: Fredrik Mertens; Bertil Johansson; Sverre Heim; Ulf Kristoffersson; Nils Mandahl; Ingemar Turesson; Claes Malm; A Othzén; C R Bartram; D Catovsky
Trisomy 14 in atypical chronic myeloid leukemia.
Leukemia 1990;4(2):117-20.
1990: Peter Elfving; J C Cigudosa; Rolf Lundgren; Janusz Limon; Nils Mandahl; Ulf Kristoffersson; Sverre Heim; Felix Mitelman
Trisomy 7, trisomy 10, and loss of the Y chromosome in short-term cultures of normal kidney tissue.
Cytogenetics and cell genetics 1990;53(2-3):123-5.
1989: Ulf Kristoffersson; Sverre Heim; Nils Mandahl; Måns Akerman; Felix Mitelman
Multiple clonal chromosome aberrations in two thymomas.
Cancer genetics and cytogenetics 1989;41(1):93-8.
1989: Rolf Lundgren; Peter Elfving; Sverre Heim; Ulf Kristoffersson; Nils Mandahl; Felix Mitelman
A squamous cell bladder carcinoma with karyotypic abnormalities reminiscent of transitional cell carcinoma.
The Journal of urology 1989;142(2 Pt 1):374-6.
1989: Janusz Limon; Rolf Lundgren; Peter Elfving; Sverre Heim; Ulf Kristoffersson; Nils Mandahl; Felix Mitelman
Double minutes in two primary adenocarcinomas of the prostate.
Cancer genetics and cytogenetics 1989;39(2):191-4.
1989: L Brandt; Ulf Kristoffersson; Håkan Olsson; Felix Mitelman
Relation between occupational exposure to organic solvents and chromosome aberrations in non-Hodgkin's lymphoma.
European journal of haematology 1989;42(3):298-302.
1988: Ulf Kristoffersson; Sverre Heim; Nils Mandahl; Håkan Olsson; Måns Akerman; Felix Mitelman
Trisomy 5 and t(5;14)(q11;q32) as the sole abnormalities in two different clones from a centroblastic non-Hodgkin's lymphoma.
Cancer genetics and cytogenetics 1988;36(2):173-6.
1988: Rolf Billström; T Thiede; S Hansen; Sverre Heim; Ulf Kristoffersson; Nils Mandahl; Felix Mitelman
Bone marrow karyotype and prognosis in primary myelodysplastic syndromes.
European journal of haematology 1988;41(4):341-6.
1988: Rolf Lundgren; Ulf Kristoffersson; Sverre Heim; Nils Mandahl; Felix Mitelman
Multiple structural chromosome rearrangements, including del(7q) and del(10q), in an adenocarcinoma of the prostate.
Cancer genetics and cytogenetics 1988;35(1):103-8.
1988: Ulf Kristoffersson; J Lagergren; Sverre Heim; Nils Mandahl
Four copies of 8p in a mentally retarded boy with the mosaic karyotype 47,XY, + i(8p)/46,XY.
Clinical genetics 1988;34(3):201-3.
1988: Felix Mitelman; E L Prigogina; E W Fleischman; M A Frenkel; Stanislaw Garwicz; Sverre Heim; G W Ilyinskaya; Ulf Kristoffersson; Nils Mandahl; M A Volkova
A new specific chromosomal rearrangement, t(11;20)(p15;q11), in myeloblastic leukemia with maturation.
Leukemia 1988;2(7):430-2.
1988: Ulf Kristoffersson; Y S Jin; Rolf Lundgren
Chromosome analysis of a newly established renal carcinoma cell line.
Cancer genetics and cytogenetics 1988;33(1):133-8.
1988: Bertil Johansson; Fredrik Mertens; L Palm; I Englesson; Ulf Kristoffersson
Duplication 18p with mild influence on the phenotype.
American journal of medical genetics 1988;29(4):871-4.
1988: Sverre Heim; Ulf Kristoffersson; Nils Mandahl; Claes Malm; Felix Mitelman
Variant translocation t(3;15)(q21;q22) in a patient with acute promyelocytic leukemia.
Leukemia 1988;2(1):65-7.
1987: Sverre Heim; Giuliana Alimena; Rolf Billström; Daniela Diverio; Ulf Kristoffersson; Nils Mandahl; M Nanni; Felix Mitelman
Tetraploid karyotype (92,XXYY) in two patients with acute lymphoblastic leukemia.
Cancer genetics and cytogenetics 1987;29(1):129-33.
1987: S Heim; Gian Carlo Avanzi; Rolf Billström; Ulf Kristoffersson; Nils Mandahl; A N Bekassy; Stanislaw Garwicz; Thomas Wiebe; L Pegoraro; Michele Falda
A new specific chromosomal rearrangement, t(8;16) (p11;p13), in acute monocytic leukaemia.
British journal of haematology 1987;66(3):323-6.
1987: Sverre Heim; A N Békàssy; Stanislaw Garwicz; J Heldrup; Thomas Wiebe; Ulf Kristoffersson; Nils Mandahl; Felix Mitelman
New structural chromosomal rearrangements in congenital leukemia.
Leukemia 1987;1(1):16-23.
1986: S Heim; Ulf Kristoffersson; Nils Mandahl; F Mitelman; A N Bekassy; Stanislaw Garwicz; J Heldrup; Thomas Wiebe
Reciprocal translocation (11;19)(q23;p13) in congenital acute lymphoblastic leukemia.
Cancer genetics and cytogenetics 1986;23(3):239-44.
1986: S Heim; Ulf Kristoffersson; Nils Mandahl; F Mitelman; A N Bekassy; Stanislaw Garwicz; Thomas Wiebe
High resolution banding analysis of the reciprocal translocation t(6;9) in acute nonlymphocytic leukemia.
Cancer genetics and cytogenetics 1986;22(3):195-201.
1985: S Heim; Rolf Billström; Ulf Kristoffersson; Nils Mandahl; Bodil Strömbeck; Felix Mitelman
Variant Ph translocations in chronic myeloid leukemia.
Cancer genetics and cytogenetics 1985;18(3):215-27.