Found: 5
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Two Swedish founder MSH6 mutations, one nonsense and one missense, conferring high cumulative risk of Lynch syndrome.
- Published in:
- Clinical Genetics, 2005, v. 68, n. 6, p. 533, doi. 10.1111/j.1399-0004.2005.00537.x
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- Publication type:
- Article
Increased levels of tPA antigen and tPA/PAI-1 complex in myotonic dystrophy.
- Published in:
- 2001
- By:
- Publication type:
- journal article
Founder effect in spinal and bulbar muscular atrophy (SBMA) in Scandinavia.
- Published in:
- European Journal of Human Genetics, 2000, v. 8, n. 8, p. 631, doi. 10.1038/sj.ejhg.5200517
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- Publication type:
- Article
P04.02 GERMLINE REARRANGEMENTS IN FAMILIES WITH STRONG FAMILY HISTORY OF GLIOMA AND MALIGNANT MELANOMA, COLON AND BREAST CANCER.
- Published in:
- Neuro-Oncology, 2014, v. 16, n. suppl_2, p. ii36, doi. 10.1093/neuonc/nou174.134
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- Publication type:
- Article
High prevalence of Kennedy's disease in Western Finland - is the syndrome underdiagnosed?
- Published in:
- Acta Neurologica Scandinavica, 1998, v. 98, n. 2, p. 128, doi. 10.1111/j.1600-0404.1998.tb01732.x
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- Publication type:
- Article