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- 2008
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Mark
Genetics in clinical practice: general practitioners' educational priorities in European countries
(
- Contribution to journal › Article
- 2007
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Mark
Report of an international survey of molecular genetic testing laboratories
(
- Contribution to journal › Article
-
Mark
Etisk argumentation och klinisk verklighet kan med fördel förenas.
(
- Contribution to journal › Article
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Mark
Brister i genetisk kunskap i vården?
2007) p.109-109(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
A hypothesis-generating search for new genetic breast cancer syndromes - a national study in 803 Swedish families
(
- Contribution to journal › Article
-
Mark
Cytogenetic Guidelines and Quality Assurance: a common European framework for quality assessment for constitutional and acquired cytogenetic investigations
(
- Contribution to journal › Article
- 2006
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Mark
Handy book on cancer genetics risk assessment
(
- Contribution to journal › Review (Book/Film/Exhibition/etc.)
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Mark
The contribution of the hereditary nonpolyposis colorectal cancer syndrome to the development of ovarian cancer.
(
- Contribution to journal › Article
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Mark
ECA Permanent working group for cytogenetics and society: Cytogenetic guidelines and quality assurance. A common framework for quality assessment for constitutional and acquired cytogenetic investigations
(
- Contribution to journal › Article
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Mark
Genetic education for non-geneticist health professionals
(
- Contribution to journal › Article
-
Mark
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
(
- Contribution to journal › Letter
-
Mark
Education in medical genetics for non-genetic health care providers in sweden.
(
- Contribution to journal › Article
- 2005
-
Mark
Genetic education and nongenetic health professionals: Educational providers and curricula in Europe.
(
- Contribution to journal › Article
-
Mark
Ny kunskap om arv och ärftlighet ger nya aspekter på hjärtsjukdom
(
- Contribution to journal › Article
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Mark
Book review: Genetic predisposition of cancer, 2nd ed.
(
- Contribution to journal › Review (Book/Film/Exhibition/etc.)
-
Mark
Nya rön om fragil X-syndromet komplicerar genetisk vägledning. Sjukdomsgenen orsakar fler symtom än vad som tidigare varit känt
(
- Contribution to journal › Article
-
Mark
Prevalence of Stroke and Vascular Risk Factors among First-Degree Relatives of Stroke Patients and Control Subjects.
(
- Contribution to journal › Article
- 2004
-
Mark
A new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG length.
(
- Contribution to journal › Article
-
Mark
One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations : results of a prospective study in Southern Sweden
(
- Contribution to journal › Article
-
Mark
External quality assessment for mutation detection in the BRCA1 and BRCA2 genes: EMQN's experience of 3 years
(
- Contribution to journal › Article
-
Mark
The need for oncogenetic counselling - Ten years' experience of a regional oncogenetic clinic
(
- Contribution to journal › Article
-
Mark
Genetisk rådgivning och fosterdiagnostik.
2004) p.56-56(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Regulation of genetic testing in clinical practice
(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
An excess of chromosome 1 breakpoints in male infertility.
(
- Contribution to journal › Article
- 2003
-
Mark
Provision of genetic service in Europe: current practices and issues.
(
- Contribution to journal › Article
-
Mark
Data storage and DNA banking for biomedical research: technical, social and ethical issues.
(
- Contribution to journal › Article
-
Mark
Lundensisk allvarshumor
(
- Contribution to journal › Review (Book/Film/Exhibition/etc.)
-
Mark
Book review: P.J. Morrison, S.V. Hodgson, N.E. Haites (eds): Familial breast cancer: genetics, screening and managementCambridge University Press, 2002, 401 pp, hardcover (ISBN 0-521-80373-X) pound 65.00.
(
- Contribution to journal › Article
-
Mark
Statens medicinsk-etiska råd. Genetisk screening - om hälsa och ärftlig sjukdomsrisk. Etiska vägmärken 11. (rec)
(
- Contribution to journal › Article
-
Mark
Ett etiskt dilemma: Farmakogenetiskt test kan ge oönskad information [An ethical dilemma: pharmacogenetic tests can yield unwanted information]
(
- Contribution to journal › Article
-
Mark
Gendiagnostik vid sjukdom – och innan den bryter ut
2003) p.31-31(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Medicinsk genetik – en introduktion.
2003)(
- Book/Report › Book
-
Mark
Population genetic screening programmes: technical, social, and ethical issues.
(
- Contribution to journal › Article
-
Mark
Provision of genetic services in Europe: current practices and issues
(
- Contribution to journal › Article
-
Mark
Genetic information and testing insurance and employment: technical, social, and ethical issues.
(
- Contribution to journal › Article
-
Mark
Ring Y chromosome in an azoospermic male with short stature: additional evidence for a distinct ring Y syndrome in non-mosaic patients?
(
- Contribution to journal › Letter
- 2002
-
Mark
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome
(
- Contribution to journal › Article
- 2001
-
Mark
Essential genetics education for non-genetics health professionals (EC Project GenEd)
(
- Contribution to journal › Article
-
Mark
Identification of human candidate genes for male infertility by digital differential display
(
- Contribution to journal › Article
-
Mark
Family history of breast and ovarian cancers and BRCA1 and BRCA2 mutations in a population-based series of early-onset breast cancer
(
- Contribution to journal › Article
-
Mark
Issues in Human GenEthics
(
- Contribution to journal › Article
-
Mark
Functional analysis of BRCA1 C-terminal missense mutations identified in breast and ovarian cancer families
(
- Contribution to journal › Article
- 2000
-
Mark
Naturvetare och kulturforskare kan överbrygga ämnesgränser
(
- Contribution to journal › Article
-
Mark
Risk perception, screening practice and interest in genetic testing among unaffected men in families with hereditary prostate cancer
(
- Contribution to journal › Article
- 1999
-
Mark
hMLH1, hMSH2 and hMSH6 mutations in hereditary non-polyposis colorectal cancer families from southern Sweden
(
- Contribution to journal › Article
-
Mark
Incidence of malignant tumours in relatives of BRCA1 and BRCA2 germline mutation carriers
(
- Contribution to journal › Article
-
Mark
Prognostic implications of cytogenetic aberrations in diffuse large B-cell lymphomas
(
- Contribution to journal › Article
-
Mark
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
(
- Contribution to journal › Article
-
Mark
Familial and hereditary prostate cancer in southern Sweden. A population-based case-control study
(
- Contribution to journal › Article
- 1998
-
Mark
Clinical course of early onset prostate cancer with special reference to family history as a prognostic factor
(
- Contribution to journal › Article