Maria Soller (Former)
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- 2015
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Mark
No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome.
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- Contribution to journal › Article
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Mark
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.
(
- Contribution to journal › Article
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Mark
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations.
2015) In European Journal of Human Genetics(
- Contribution to journal › Article
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Mark
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
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- Contribution to journal › Article
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Mark
The gynecological surveillance of women with Lynch syndrome in Sweden.
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- Contribution to journal › Article
- 2014
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Mark
Atypical Friedreich ataxia in patients with FXN p.R165P point mutation or comorbid hemochromatosis.
(
- Contribution to journal › Article
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Mark
Autosomal dominant cerebellar ataxia with slow ocular saccades, neuropathy and orthostatism: A novel entity?
(
- Contribution to journal › Article
- 2013
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Mark
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
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- Contribution to journal › Article
- 2012
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Mark
Relation between smoking history and gene expression profiles in lung adenocarcinomas
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- Contribution to journal › Article
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Mark
Friedreich ataxia in patients with FXN p.R165P point mutation.
(
- Contribution to journal › Published meeting abstract