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- 2003
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Mark
A genome wide scan for early onset primary hypertension in Scandinavians.
(
- Contribution to journal › Article
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Mark
Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma
(
- Contribution to journal › Article
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Mark
High resolution mapping of an arthritis susceptibility locus on rat chromosome 4, and characterization of regulated phenotypes
(
- Contribution to journal › Article
- 2002
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Mark
Impaired dopamine storage resulting from alpha-synuclein mutations may contribute to the pathogenesis of Parkinson's disease.
(
- Contribution to journal › Scientific review
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Mark
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications.
(
- Contribution to journal › Article
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Mark
Linkage disequilibrium between polymorphisms in the human TNFRSF1B gene and their association with bone mass in perimenopausal women
(
- Contribution to journal › Article
- 2001
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Mark
X chromosome-specific cDNA arrays: identification of genes that escape from X-inactivation and other applications
(
- Contribution to journal › Article
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Mark
Fusion of the MORF and CBP genes in acute myeloid leukemia with the t(10;16)(q22;p13)
(
- Contribution to journal › Article
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Mark
DNA methylation patterns in hereditary human cancers mimic sporadic tumorigenesis
(
- Contribution to journal › Article
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Mark
The mutational spectrum of human malignant autosomal recessive osteopetrosis
(
- Contribution to journal › Article