nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A Combinatorial Approach to Detecting Gene-Gene and Gene-Environment Interactions in Family Studies
|
Lou, Xiang-Yang |
|
2008 |
83 |
4 |
p. 457-467 11 p. |
artikel |
2 |
A Connective Tissue Disorder Caused by Mutations of the Lysyl Hydroxylase 3 Gene
|
Salo, Antti M. |
|
2008 |
83 |
4 |
p. 495-503 9 p. |
artikel |
3 |
Civilian and Military Genetics: Nondiscrimination Policy in a Post-GINA World
|
Baruch, Susannah |
|
2008 |
83 |
4 |
p. 435-444 10 p. |
artikel |
4 |
Comparing Algorithms for Genotype Imputation
|
Marchini, Jonathan |
|
2008 |
83 |
4 |
p. 535-539 5 p. |
artikel |
5 |
HLA-DRB1∗0401 and HLA-DRB1∗0408 Are Strongly Associated with the Development of Antibodies against Interferon-β Therapy in Multiple Sclerosis
|
Hoffmann, Steve |
|
2008 |
83 |
4 |
p. 541- 1 p. |
artikel |
6 |
Japanese Population Structure, Based on SNP Genotypes from 7003 Individuals Compared to Other Ethnic Groups: Effects on Population-Based Association Studies
|
Yamaguchi-Kabata, Yumi |
|
2008 |
83 |
4 |
p. 445-456 12 p. |
artikel |
7 |
Mutation of C20orf7 Disrupts Complex I Assembly and Causes Lethal Neonatal Mitochondrial Disease
|
Sugiana, Canny |
|
2008 |
83 |
4 |
p. 468-478 11 p. |
artikel |
8 |
Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome
|
Kim, Hyung-Goo |
|
2008 |
83 |
4 |
p. 511-519 9 p. |
artikel |
9 |
Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood
|
Zeharia, Avraham |
|
2008 |
83 |
4 |
p. 489-494 6 p. |
artikel |
10 |
[No title]
|
|
|
2008 |
83 |
4 |
p. 542- 1 p. |
artikel |
11 |
Population-Based Genome-wide Association Studies Reveal Six Loci Influencing Plasma Levels of Liver Enzymes
|
Yuan, Xin |
|
2008 |
83 |
4 |
p. 520-528 9 p. |
artikel |
12 |
Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients
|
Vrijenhoek, Terry |
|
2008 |
83 |
4 |
p. 504-510 7 p. |
artikel |
13 |
Reply to Marchini and Howie
|
Lin, D.Y. |
|
2008 |
83 |
4 |
p. 539-540 2 p. |
artikel |
14 |
Targeting Dyrk1A with AAVshRNA Attenuates Motor Alterations in TgDyrk1A, a Mouse Model of Down Syndrome
|
Ortiz-Abalia, Jon |
|
2008 |
83 |
4 |
p. 479-488 10 p. |
artikel |
15 |
The H Syndrome Is Caused by Mutations in the Nucleoside Transporter hENT3
|
Molho-Pessach, Vered |
|
2008 |
83 |
4 |
p. 529-534 6 p. |
artikel |
16 |
This Month in Genetics
|
Garber, Kathryn B. |
|
2008 |
83 |
4 |
p. 433-434 2 p. |
artikel |
17 |
This Month in The Journal
|
Williamson, Robin E. |
|
2008 |
83 |
4 |
p. 431-432 2 p. |
artikel |