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- 2017
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Mark
Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in Humans
(
- Contribution to journal › Article
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Mark
Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis
(
- Contribution to journal › Article
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Mark
Parental responsibility in the context of neuroscience and genetics
Hens, Kristien ; Cutas, Daniela LU and Horstkötter, Dorothee (2017)
- Book/Report › Anthology (editor)
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Mark
Genetic determinants of growth hormone and GH-related phenotypes
(
- Contribution to journal › Article
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Mark
GISCOME – Genetics of Ischaemic Stroke Functional Outcome network : A protocol for an international multicentre genetic association study
(
- Contribution to journal › Article
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Mark
Novel APC gene mutations associated with protein alteration in diffuse type gastric cancer
(
- Contribution to journal › Article
- 2016
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Mark
A Variant of GJD2, Encoding for Connexin 36, Alters the Function of Insulin Producing β-Cells.
(
- Contribution to journal › Article
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Mark
Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels.
(
- Contribution to journal › Article
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Mark
A somatic mutation of GFI1B identified in leukemia alters cell fate via a SPI1 (PU.1) centered genetic regulatory network.
(
- Contribution to journal › Article
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Mark
An update of a classical textbook.
(
- Contribution to journal › Review (Book/Film/Exhibition/etc.)