Division of Clinical Genetics
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- 2002
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Mark
Chordoma
2002) p.316-316(
- Chapter in Book/Report/Conference proceeding › Book chapter
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Mark
Enchondromatosis: Ollier disease and Maffucci syndrome
2002) p.356-356(
- Chapter in Book/Report/Conference proceeding › Book chapter
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Mark
Congenital and inherited syndromes associated with bone and soft tissue tumours
2002) p.349-349(
- Chapter in Book/Report/Conference proceeding › Book chapter
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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
Molecular genetic characterization of the EWS/CHN and RBP56/CHN fusion genes in extraskeletal myxoid chondrosarcoma.
(
- Contribution to journal › Article
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Mark
Involvement and functional impairment of the CD34(+)CD38(-)Thy-1(+) hematopoietic stem cell pool in myelodysplastic syndromes with trisomy 8.
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- Contribution to journal › Article
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Mark
Frequent amplification of 8q24, 11q, 17q, and 20q-specific genes in pancreatic cancer
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- Contribution to journal › Article
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Mark
Correlation between clinicopathological features and karyotype in 100 cartilaginous and chordoid tumours. A report from the Chromosomes and Morphology (CHAMP) Collaborative Study Group
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- Contribution to journal › Article
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Mark
Co-existence of SYT-SSX1 and SYT-SSX2 fusions in synovial sarcomas
(
- Contribution to journal › Article
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Mark
Centrosomal abnormalities, multipolar mitoses, and chromosomal instability in head and neck tumours with dysfunctional telomeres.
(
- Contribution to journal › Article