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- 2004
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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.
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- Contribution to journal › Article
-
Mark
Deficiency of GDP-Man:GlcNAc2-PP-Dolichol Mannosyltransferase Causes Congenital Disorder of Glycosylation Type Ik
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- Contribution to journal › Article
- 2003
-
Mark
Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: A combined analysis of 22 studies
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- Contribution to journal › Article
-
Mark
A novel chromosomal translocation t(3;7)(q26;q21) in myeloid leukemia resulting in overexpression of EVI1
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- Contribution to journal › Published meeting abstract
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Mark
Localization of a novel melanoma susceptibility locus to 1p22
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- Contribution to journal › Article
- 2002
-
Mark
A variation in 3 ' UTR of hPTP1B increases specific gene expression and associates with insulin resistance
(
- Contribution to journal › Article
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Mark
GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1L
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- Contribution to journal › Article
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Mark
Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia study.
(
- Contribution to journal › Article
- 2001
-
Mark
Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height
(
- Contribution to journal › Article
-
Mark
SR-B1 variants associated with HDL cholesterol levels in three populations
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- Contribution to journal › Article