| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Comparative Analysis of the Genetic Epidemiology of Deafness in the United States in Two Sets of Pedigrees Collected More than a Century Apart
|
Arnos, Kathleen S.
|
|
2008
|
83 |
2 |
p. 200-207
8 p.
|
artikel
|
| 2 |
An Algorithm for Inferring Complex Haplotypes in a Region of Copy-Number Variation
|
Kato, Mamoru
|
|
2008
|
83 |
2 |
p. 157-169
13 p.
|
artikel
|
| 3 |
ATM Gene Mutations Result in Both Recessive and Dominant Expression Phenotypes of Genes and MicroRNAs
|
Smirnov, Denis A.
|
|
2008
|
83 |
2 |
p. 243-253
11 p.
|
artikel
|
| 4 |
Class-Specific Correlations of Gene Expressions: Identification and Their Effects on Clustering Analyses
|
Zhang, Jigang
|
|
2008
|
83 |
2 |
p. 269-277
9 p.
|
artikel
|
| 5 |
Congenital Joint Dislocations Caused by Carbohydrate Sulfotransferase 3 Deficiency in Recessive Larsen Syndrome and Humero-Spinal Dysostosis
|
Hermanns, Pia
|
|
2008
|
83 |
2 |
p. 293-
1 p.
|
artikel
|
| 6 |
Evolutionary Forces Shape the Human RFPL1,2,3 Genes toward a Role in Neocortex Development
|
Bonnefont, Jérôme
|
|
2008
|
83 |
2 |
p. 208-218
11 p.
|
artikel
|
| 7 |
Extensive Copy-Number Variation of the Human Olfactory Receptor Gene Family
|
Young, Janet M.
|
|
2008
|
83 |
2 |
p. 228-242
15 p.
|
artikel
|
| 8 |
Germline Mutations and Variants in the Succinate Dehydrogenase Genes in Cowden and Cowden-like Syndromes
|
Ni, Ying
|
|
2008
|
83 |
2 |
p. 261-268
8 p.
|
artikel
|
| 9 |
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 |
2 |
p. 219-227
9 p.
|
artikel
|
| 10 |
Impairment of SLC17A8 Encoding Vesicular Glutamate Transporter-3, VGLUT3, Underlies Nonsyndromic Deafness DFNA25 and Inner Hair Cell Dysfunction in Null Mice
|
Ruel, Jérôme
|
|
2008
|
83 |
2 |
p. 278-292
15 p.
|
artikel
|
| 11 |
Maternally Inherited Birk Barel Mental Retardation Dysmorphism Syndrome Caused by a Mutation in the Genomically Imprinted Potassium Channel KCNK9
|
Barel, Ortal
|
|
2008
|
83 |
2 |
p. 193-199
7 p.
|
artikel
|
| 12 |
Mutations in the Cilia Gene ARL13B Lead to the Classical Form of Joubert Syndrome
|
Cantagrel, Vincent
|
|
2008
|
83 |
2 |
p. 170-179
10 p.
|
artikel
|
| 13 |
Neuropsychological Endophenotype Approach to Genome-wide Linkage Analysis Identifies Susceptibility Loci for ADHD on 2q21.1 and 13q12.11
|
Rommelse, Nanda N.J.
|
|
2008
|
83 |
2 |
p. 294-
1 p.
|
artikel
|
| 14 |
[No title]
|
|
|
2008
|
83 |
2 |
p. 295-296
2 p.
|
artikel
|
| 15 |
Pathogenic Mitochondrial DNA Mutations Are Common in the General Population
|
Elliott, Hannah R.
|
|
2008
|
83 |
2 |
p. 254-260
7 p.
|
artikel
|
| 16 |
This Month in Genetics
|
Garber, Kathryn B.
|
|
2008
|
83 |
2 |
p. 155-156
2 p.
|
artikel
|
| 17 |
This Month in The Journal
|
Williamson, Robin E.
|
|
2008
|
83 |
2 |
p. 153-154
2 p.
|
artikel
|
| 18 |
WW-Domain-Containing Oxidoreductase Is Associated with Low Plasma HDL-C Levels
|
Lee, Jenny C.
|
|
2008
|
83 |
2 |
p. 180-192
13 p.
|
artikel
|
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