| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Distinct DNA-Methylation Boundary in the 5′- Upstream Sequence of the FMR1 Promoter Binds Nuclear Proteins and Is Lost in Fragile X Syndrome
|
Naumann, Anja
|
|
2010
|
86 |
1 |
p. 98-100
3 p.
|
artikel
|
| 2 |
A Major Determinant for Binding and Aminoacylation of tRNAAla in Cytoplasmic Alanyl-tRNA Synthetase Is Mutated in Dominant Axonal Charcot-Marie-Tooth Disease
|
Latour, Philippe
|
|
2010
|
86 |
1 |
p. 77-82
6 p.
|
artikel
|
| 3 |
Announcements
|
|
|
2010
|
86 |
1 |
p. 101-102
2 p.
|
artikel
|
| 4 |
Autosomal-Dominant Striatal Degeneration Is Caused by a Mutation in the Phosphodiesterase 8B Gene
|
Appenzeller, Silke
|
|
2010
|
86 |
1 |
p. 83-87
5 p.
|
artikel
|
| 5 |
Highly Punctuated Patterns of Population Structure on the X Chromosome and Implications for African Evolutionary History
|
Lambert, Charla A.
|
|
2010
|
86 |
1 |
p. 34-44
11 p.
|
artikel
|
| 6 |
Identification of KCNJ15 as a Susceptibility Gene in Asian Patients with Type 2 Diabetes Mellitus
|
Okamoto, Koji
|
|
2010
|
86 |
1 |
p. 54-64
11 p.
|
artikel
|
| 7 |
Joubert Syndrome 2 (JBTS2) in Ashkenazi Jews Is Associated with a TMEM216 Mutation
|
Edvardson, Simon
|
|
2010
|
86 |
1 |
p. 93-97
5 p.
|
artikel
|
| 8 |
Leveraging Genetic Variability across Populations for the Identification of Causal Variants
|
Zaitlen, Noah
|
|
2010
|
86 |
1 |
p. 23-33
11 p.
|
artikel
|
| 9 |
Loss-of-Function Mutations in the PRPS1 Gene Cause a Type of Nonsyndromic X-linked Sensorineural Deafness, DFN2
|
Liu, Xuezhong
|
|
2010
|
86 |
1 |
p. 65-71
7 p.
|
artikel
|
| 10 |
Missense Mutations in TCF8 Cause Late-Onset Fuchs Corneal Dystrophy and Interact with FCD4 on Chromosome 9p
|
Riazuddin, S. Amer
|
|
2010
|
86 |
1 |
p. 45-53
9 p.
|
artikel
|
| 11 |
Prioritizing GWAS Results: A Review of Statistical Methods and Recommendations for Their Application
|
Cantor, Rita M.
|
|
2010
|
86 |
1 |
p. 6-22
17 p.
|
artikel
|
| 12 |
Quantitative Trait Loci for CD4:CD8 Lymphocyte Ratio Are Associated with Risk of Type 1 Diabetes and HIV-1 Immune Control
|
Ferreira, Manuel A.R.
|
|
2010
|
86 |
1 |
p. 88-92
5 p.
|
artikel
|
| 13 |
Targeted Next-Generation Sequencing Appoints C16orf57 as Clericuzio-Type Poikiloderma with Neutropenia Gene
|
Volpi, Ludovica
|
|
2010
|
86 |
1 |
p. 72-76
5 p.
|
artikel
|
| 14 |
This Month in Genetics
|
Garber, Kathryn B.
|
|
2010
|
86 |
1 |
p. 3-5
3 p.
|
artikel
|
| 15 |
This Month in The Journal
|
Bungartz, Kathryn D.
|
|
2010
|
86 |
1 |
p. 1-2
2 p.
|
artikel
|
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