Anna Collin (Former)
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- 2018
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Mark
Generation of a human induced pluripotent stem cell line (CSC-42) from a patient with sporadic form of Parkinson's disease
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- Contribution to journal › Article
- 2013
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Mark
Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumor.
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- Contribution to journal › Article
- 2012
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Mark
Report from the European Myeloma Network on interphase FISH in multiple myeloma and related disorders
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- Contribution to journal › Article
- 2010
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Mark
dup(19)(q12q13.2): Array-based Genotype-Phenotype Correlation of a New Possibly Obesity-related Syndrome.
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- Contribution to journal › Article
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Mark
Characterization of an alternative transcript of the human CREB3L2 gene.
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- Contribution to journal › Article
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Mark
Fusion of the FUS and CREB3L2 genes in a supernumerary ring chromosome in low-grade fibromyxoid sarcoma.
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- Contribution to journal › Article
- 2009
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Mark
Clinical Variability of Waardenburg-Shah Syndrome in Patients With Proximal 13q Deletion Syndrome Including the Endothelin-B Receptor Locus
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- Contribution to journal › Article
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Mark
False-positive prenatal diagnosis of trisomy 18 by interphase FISH: hybridization of chromosome 18 alpha-satellite probe (D18Z1) to chromosome 2.
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- Contribution to journal › Article
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Mark
Expression levels of HMGA2 in adipocytic tumors correlate with morphologic and cytogenetic subgroups.
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- Contribution to journal › Article
- 2008
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Mark
Array-based genotype-phenotype correlation in a case of supernumerary ring chromosome 12
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- Contribution to journal › Article