Division of Clinical Genetics
991 – 1000 of 1291
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2004
-
Mark
Amplification of chromosome 1 sequences in lipomatous tumors and other sarcomas
(
- Contribution to journal › Article
-
Mark
Identification of cytogenetic subgroups and karyotypic pathways of clonal evolution in follicular lymphomas.
(
- Contribution to journal › Article
-
Mark
A model for karyotypic evolution in testicular germ cell tumors.
(
- Contribution to journal › Article
-
Mark
High frequencies of chromosomal aberrations in multiple myeloma and monoclonal gammopathy of undetermined significance in direct chromosome preparation.
(
- Contribution to journal › Article
-
Mark
Dissecting karyotypic patterns in malignant melanomas: Temporal clustering of losses and gains in melanoma karyotypic evolution.
(
- Contribution to journal › Article
-
Mark
Amylin inhibits bone resorption while the calcitonin receptor controls bone formation in vivo
(
- Contribution to journal › Article
-
Mark
A new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG length.
(
- Contribution to journal › Article
-
Mark
Identification of a commonly amplified 4.3 Mb region with overexpression of the C8FW gene, encoding a phosphoprotein regulated by mitogenic pathways, but not of the MYC gene in MYC-containing double minutes in myeloid malignancies.
(
- Contribution to journal › Article
-
Mark
The Breakpoint Region of the Most Common Isochromosome, i(17q), in Human Neoplasia Is Characterized by a Complex Genomic Architecture with Large, Palindromic, Low-Copy Repeats.
(
- Contribution to journal › Article
-
Mark
Structural integrity and expression of the L3MBTL gene in normal and malignant hematopoietic cells
(
- Contribution to journal › Article