1 – 10 of 14
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2021
-
Mark
A search for modifying genetic factors in CHEK2:c.1100delC breast cancer patients
(
- Contribution to journal › Article
- 2018
-
Mark
ABO genotyping with next-generation sequencing to resolve heterogeneity in donors with serology discrepancies
(
- Contribution to journal › Article
- 2011
-
Mark
High-resolution genomic screening in mantle cell lymphoma--specific changes correlate with genomic complexity, the proliferation signature and survival.
(
- Contribution to journal › Article
-
Mark
A Tunisian patient with Pearson syndrome harboring the 4.977kb common deletion associated to two novel large-scale mitochondrial deletions
(
- Contribution to journal › Article
-
Mark
Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers
(
- Contribution to journal › Article
- 2010
-
Mark
A case of Kearns-Sayre syndrome with two novel deletions (9.768 and 7.253 kb) of the mtDNA associated with the common deletion in blood leukocytes, buccal mucosa and hair follicles
(
- Contribution to journal › Article
- 2008
-
Mark
Functional importance of individual rRNA 2'-O-ribose methylations revealed by high-resolution phenotyping
(
- Contribution to journal › Article
-
Mark
An investigation into whether deletions in 9p reflect prognosis in adult precursor B-cell acute lymphoblastic leukemia : a multi-center study of 381 patients
(
- Contribution to journal › Article
- 2005
-
Mark
Fusion of the EWSR1 and ATF1 genes without expression of the MITF-M transcript in angiomatoid fibrous histiocytoma
(
- Contribution to journal › Article
- 2000
-
Mark
Molecular analysis of FRIGIDA, a major determinant of natural variation in Arabidopsis flowering time
(
- Contribution to journal › Article