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- 2014
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Mark
Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum
(
- Contribution to journal › Article
- 2013
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Mark
Risk of thyroid cancer in first-degree relatives of patients with non-medullary thyroid cancer by histology type and age at diagnosis: a joint study from five Nordic countries
(
- Contribution to journal › Article
- 2012
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Mark
BRCA1 R1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer risk
(
- Contribution to journal › Article
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Mark
A genome-wide association study of men with symptoms of testicular dysgenesis syndrome and its network biology interpretation
(
- Contribution to journal › Article
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Mark
Prostate cancer risk assessment model: a scoring model based on the Swedish Family-Cancer Database
(
- Contribution to journal › Article
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Mark
Closing the case of APOE in multiple sclerosis : no association with disease risk in over 29 000 subjects
(
- Contribution to journal › Article
- 2008
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Mark
Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation
(
- Contribution to journal › Article
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Mark
A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome
(
- Contribution to journal › Article
- 2007
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Mark
Germline E-cadherin mutations in familial lobular breast cancer
(
- Contribution to journal › Article
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Mark
Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents
(
- Contribution to journal › Article