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- 2008
-
Mark
Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delay.
(
- Contribution to journal › Article
- 2007
-
Mark
A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study
(
- Contribution to journal › Article
-
Mark
Mutation analysis of the NSD1 gene in patients with autism spectrum disorders and macrocephaly
(
- Contribution to journal › Article
-
Mark
CT60 genotype does not affect CTLA-4 isoform expression despite association to TID and AITD in northern Sweden
(
- Contribution to journal › Article
- 2006
-
Mark
Multilevel analysis of systolic blood pressure and ACE gene I/D polymorphism in 438 Swedish families - a public health perspective
(
- Contribution to journal › Article
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