101 – 110 of 116
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2003
-
Mark
A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2-q22 linked to type 2 diabetes.
(
- Contribution to journal › Article
-
Mark
Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma
(
- Contribution to journal › Article
-
Mark
Gene expression profile in multiple sclerosis patients and healthy controls: identifying pathways relevant to disease
(
- Contribution to journal › Article
- 2002
-
Mark
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications.
(
- Contribution to journal › Article
-
Mark
Impaired dopamine storage resulting from alpha-synuclein mutations may contribute to the pathogenesis of Parkinson's disease.
(
- Contribution to journal › Scientific review
-
Mark
Linkage disequilibrium between polymorphisms in the human TNFRSF1B gene and their association with bone mass in perimenopausal women
(
- Contribution to journal › Article
- 2001
-
Mark
Functional analysis of BRCA1 C-terminal missense mutations identified in breast and ovarian cancer families
(
- Contribution to journal › Article
-
Mark
Fusion of the MORF and CBP genes in acute myeloid leukemia with the t(10;16)(q22;p13)
(
- Contribution to journal › Article
-
Mark
X chromosome-specific cDNA arrays: identification of genes that escape from X-inactivation and other applications
(
- Contribution to journal › Article
-
Mark
The mutational spectrum of human malignant autosomal recessive osteopetrosis
(
- Contribution to journal › Article