1731 – 1740 of 1918
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- 2001
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Mark
Bioinformatics in proteomics
(
- Contribution to journal › Scientific review
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Mark
Extensive cytogenetic heterogeneity in a benign retroperitoneal schwannoma
(
- Contribution to journal › Article
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Mark
Analysis of short stature homeobox-containing gene ( SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity
(
- Contribution to journal › Article
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Mark
BRCA1 and BRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young age
(
- Contribution to journal › Article
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Mark
Cytogenetic and fluorescence in situ hybridization characterization of chromosome 8 rearrangements in head and neck squamous cell carcinomas
(
- Contribution to journal › Article
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Mark
Cloning of the der(17)t(X;17)(p11;q25) of alveolar soft part sarcoma identifies the ASPL-TFE3 gene fusion, a new molecular diagnostic marker
(
- Contribution to journal › Article
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Mark
Analysis of the distribution and frequency of trisomy 7 in vivo in synovia from patients with osteoarthritis and pigmented villonodular synovitis
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- Contribution to journal › Article
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Mark
The incidence of trisomy 8 as a sole chromosomal aberration in myeloid malignancies varies in relation to gender, age, prior iatrogenic genotoxic exposure, and morphology
(
- Contribution to journal › Article
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Mark
4 Primary immunodeficiency mutation databases
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- Contribution to journal › Scientific review
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Mark
Refined characterisation of chromosome aberrations in tumours by multicolour banding and electronic mapping resources
2001) In Methods in cell science: an official journal of the Society for In Vitro Biology 23(1-3). p.23-28(
- Contribution to journal › Article