1 – 5 of 5
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2012
-
Mark
Evaluation of chromosome 6p22 as a breast cancer risk modifier locus in a follow-up study of BRCA2 mutation carriers
(
- Contribution to journal › Article
- 2009
-
Mark
The HBS1L-MYB intergenic interval associated with elevated HbF levels shows characteristics of a distal regulatory region in erythroid cells
(
- Contribution to journal › Article
- 2007
-
Mark
Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults
2007) In Proceedings of the National Academy of Sciences of the United States of America 104(27). p.51-11346(
- Contribution to journal › Article
- 2006
-
Mark
Chromosome aberrations including der(6)t(2;6)(p15;p21.3) and der(22)t(3;22)(p21;p11) in the evolution of essential thrombocythemia to myelofibrosis with myeloid metaplasia
(
- Contribution to journal › Article
- 2002
-
Mark
Allelic loss in clinically and screening-detected primary hyperparathyroidism
(
- Contribution to journal › Article