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- 2006
-
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
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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
- 2005
-
Mark
Prevalence of Stroke and Vascular Risk Factors among First-Degree Relatives of Stroke Patients and Control Subjects.
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- Contribution to journal › Article
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Mark
Genetic education and nongenetic health professionals: Educational providers and curricula in Europe.
(
- Contribution to journal › Article
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Mark
Book review: Genetic predisposition of cancer, 2nd ed.
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- Contribution to journal › Review (Book/Film/Exhibition/etc.)
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Mark
Nya rön om fragil X-syndromet komplicerar genetisk vägledning. Sjukdomsgenen orsakar fler symtom än vad som tidigare varit känt
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- Contribution to journal › Article
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Mark
Ny kunskap om arv och ärftlighet ger nya aspekter på hjärtsjukdom
(
- Contribution to journal › Article
- 2004
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Mark
A new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG length.
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- Contribution to journal › Article
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Mark
An excess of chromosome 1 breakpoints in male infertility.
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- Contribution to journal › Article