nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
An Alu repeat-mediated genomic GCNT2 deletion underlies congenital cataracts and adult i blood group
|
Borck, Guntram |
|
2011 |
131 |
2 |
p. 209-216 |
artikel |
2 |
Analysis of family- and population-based samples in cohort genome-wide association studies
|
Manichaikul, Ani |
|
2011 |
131 |
2 |
p. 275-287 |
artikel |
3 |
A novel transcript of cyclin-dependent kinase-like 5 (CDKL5) has an alternative C-terminus and is the predominant transcript in brain
|
Williamson, Sarah L. |
|
2011 |
131 |
2 |
p. 187-200 |
artikel |
4 |
Functional haplotypes of Fc gamma (Fcγ) receptor (FcγRIIA and FcγRIIIB) predict risk to repeated episodes of severe malarial anemia and mortality in Kenyan children
|
Ouma, Collins |
|
2011 |
131 |
2 |
p. 289-299 |
artikel |
5 |
Functional haplotypes of Fc gamma (Fcγ) receptor (FcγRIIA and FcγRIIIB) predict risk to repeated episodes of severe malarial anemia and mortality in Kenyan children
|
Ouma, Collins |
|
|
131 |
2 |
p. 289-299 |
artikel |
6 |
Meta-analysis of new genome-wide association studies of colorectal cancer risk
|
Peters, Ulrike |
|
2011 |
131 |
2 |
p. 217-234 |
artikel |
7 |
Michelle Webb (ed): Cancer Susceptibility: Methods and Protocols
|
Alsaegh, Abeer |
|
2011 |
131 |
2 |
p. 315-316 |
artikel |
8 |
Missense substitutions in the GAS1 protein present in holoprosencephaly patients reduce the affinity for its ligand, SHH
|
Pineda-Alvarez, Daniel E. |
|
2011 |
131 |
2 |
p. 301-310 |
artikel |
9 |
Mitochondrial DNA and inflammatory diseases
|
Escames, Germaine |
|
2011 |
131 |
2 |
p. 161-173 |
artikel |
10 |
Mitochondrial Haplogroup X is associated with successful aging in the Amish
|
Courtenay, Monique D. |
|
2011 |
131 |
2 |
p. 201-208 |
artikel |
11 |
Preimplantation genetic diagnosis: State of the ART 2011
|
Harper, Joyce C. |
|
2011 |
131 |
2 |
p. 175-186 |
artikel |
12 |
Studies in a consanguineous family reveal a novel locus for stuttering on chromosome 16q
|
Raza, Muhammad Hashim |
|
2011 |
131 |
2 |
p. 311-313 |
artikel |
13 |
Successful COG8 and PDF overlap is mediated by alterations in splicing and polyadenylation signals
|
Pereira-Castro, Isabel |
|
2011 |
131 |
2 |
p. 265-274 |
artikel |
14 |
The cell adhesion gene PVRL3 is associated with congenital ocular defects
|
Lachke, Salil A. |
|
2011 |
131 |
2 |
p. 235-250 |
artikel |
15 |
The impact of Converso Jews on the genomes of modern Latin Americans
|
Velez, C. |
|
2011 |
131 |
2 |
p. 251-263 |
artikel |