| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Admixture in Mexico City: implications for admixture mapping of Type 2 diabetes genetic risk factors
|
Martinez-Marignac, Veronica L.
|
|
2006
|
120 |
6 |
p. 807-819
|
artikel
|
| 2 |
A novel polymorphism associated with lactose tolerance in Africa: multiple causes for lactase persistence?
|
Ingram, Catherine J. E.
|
|
2006
|
120 |
6 |
p. 779-788
|
artikel
|
| 3 |
Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2–q13.3
|
Khan, Shahid Y.
|
|
2006
|
120 |
6 |
p. 789-793
|
artikel
|
| 4 |
Cytogenetically balanced translocations are associated with focal copy number alterations
|
Watson, Spencer K.
|
|
2006
|
120 |
6 |
p. 795-805
|
artikel
|
| 5 |
Evidence for statistical epistasis between catechol-O-methyltransferase (COMT) and polymorphisms in RGS4, G72 (DAOA), GRM3, and DISC1: influence on risk of schizophrenia
|
Nicodemus, Kristin K.
|
|
2006
|
120 |
6 |
p. 889-906
|
artikel
|
| 6 |
Friedrich Vogel 1925–2006
|
Propping, Peter
|
|
|
120 |
6 |
p. 751-753
|
artikel
|
| 7 |
Friedrich Vogel 1925–2006
|
Propping, Peter
|
|
2006
|
120 |
6 |
p. 751-753
|
artikel
|
| 8 |
Identification of a regulatory SNP in the retinol binding protein 4 gene associated with type 2 diabetes in Mongolia
|
Munkhtulga, Lkhagvasuren
|
|
2006
|
120 |
6 |
p. 879-888
|
artikel
|
| 9 |
Mitochondrial haplogroup N9b is protective against myocardial infarction in Japanese males
|
Nishigaki, Yutaka
|
|
2006
|
120 |
6 |
p. 827-836
|
artikel
|
| 10 |
Molecular characterization of deletion breakpoints in adults with 22q11 deletion syndrome
|
Weksberg, Rosanna
|
|
2006
|
120 |
6 |
p. 837-845
|
artikel
|
| 11 |
My last visit with Friedrich Vogel: a personal remembrance
|
Rappold, Gudrun
|
|
|
120 |
6 |
p. 749-750
|
artikel
|
| 12 |
My last visit with Friedrich Vogel: a personal remembrance
|
Rappold, Gudrun
|
|
2006
|
120 |
6 |
p. 749-750
|
artikel
|
| 13 |
Novel human pathological mutations
|
|
|
2006
|
120 |
6 |
p. 907-918
|
artikel
|
| 14 |
Obituary: Prof. Dr. med. Dr. h. c. Friedrich Vogel (1925–2006)
|
Sperling, Karl
|
|
|
120 |
6 |
p. 755-757
|
artikel
|
| 15 |
Obituary: Prof. Dr. med. Dr. h. c. Friedrich Vogel (1925–2006)
|
Sperling, Karl
|
|
2006
|
120 |
6 |
p. 755-757
|
artikel
|
| 16 |
Sequence variant in the laminin γ1 (LAMC1) gene associated with familial pelvic organ prolapse
|
Nikolova, Ganka
|
|
2006
|
120 |
6 |
p. 847-856
|
artikel
|
| 17 |
Structural divergence between the human and chimpanzee genomes
|
Kehrer-Sawatzki, Hildegard
|
|
2006
|
120 |
6 |
p. 759-778
|
artikel
|
| 18 |
Subsets of SNPs define rare genotype classes that predict ischemic heart disease
|
Frikke-Schmidt, Ruth
|
|
2006
|
120 |
6 |
p. 865-877
|
artikel
|
| 19 |
The LRRK2 Gly2385Arg variant is associated with Parkinson’s disease: genetic and functional evidence
|
Tan, E. K.
|
|
2006
|
120 |
6 |
p. 857-863
|
artikel
|
| 20 |
The possible role of 10398A and 16189C mtDNA variants in providing susceptibility toT2DM in two North Indian populations: a replicative study
|
Bhat, Audesh
|
|
2006
|
120 |
6 |
p. 821-826
|
artikel
|
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