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- 2011
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Mark
Ultrasonographic findings in spontaneous miscarriage: relation to euploidy and aneuploidy
(
- Contribution to journal › Article
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Mark
Fusion Gene Microarray Reveals Cancer Type-Specificity Among Fusion Genes
(
- Contribution to journal › Article
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Mark
Mutation Update for the PORCN Gene
(
- Contribution to journal › Article
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Mark
Biparental inheritance of chromosomal abnormalities in male twins with non-syndromic mental retardation
(
- Contribution to journal › Article
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Mark
Amplification of the G allele at SNP rs6983267 in 8q24 amplicons in myeloid malignancies as cause of the lack of MYC overexpression?
(
- Contribution to journal › Letter
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Mark
Identification of a Novel, Recurrent HEY1-NCOA2 Fusion in Mesenchymal Chondrosarcoma Based on a Genome-Wide Screen of Exon-Level Expression Data
2011) Annual Meeting on the United States and Canadian-Academy-of-Pathology, 2011 In Laboratory Investigation 91. p.23-23(
- Contribution to journal › Published meeting abstract
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Mark
Malignant Fibrous Histiocytoma and Fibrosarcoma of Bone in 2011: What's New?
2011) Annual Meeting on the United States and Canadian-Academy-of-Pathology, 2011 In Laboratory Investigation 91. p.20-20(
- Contribution to journal › Published meeting abstract
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Mark
Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2
(
- Contribution to journal › Article
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Mark
A large deletion identified in a Swedish family with type 1 VWD
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- Contribution to journal › Letter
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Mark
Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome
(
- Contribution to journal › Article