| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Test for Genetic Association that Incorporates Information about Deviation from Hardy-Weinberg Proportions in Cases
|
Wang, Jian
|
|
2008
|
83 |
1 |
p. 53-63
11 p.
|
artikel
|
| 2 |
East Asian and Melanesian Ancestry in Polynesians
|
Hedrick, Philip
|
|
2008
|
83 |
1 |
p. 139-140
2 p.
|
artikel
|
| 3 |
Employment Opportunities
|
|
|
2008
|
83 |
1 |
p. 150-151
2 p.
|
artikel
|
| 4 |
Evaluating the Effects of Imputation on the Power, Coverage, and Cost Efficiency of Genome-wide SNP Platforms
|
Anderson, Carl A.
|
|
2008
|
83 |
1 |
p. 112-119
8 p.
|
artikel
|
| 5 |
FOXG1 Is Responsible for the Congenital Variant of Rett Syndrome
|
Ariani, Francesca
|
|
2008
|
83 |
1 |
p. 89-93
5 p.
|
artikel
|
| 6 |
Fragile X-Related Proteins Regulate Mammalian Circadian Behavioral Rhythms
|
Zhang, Jing
|
|
2008
|
83 |
1 |
p. 43-52
10 p.
|
artikel
|
| 7 |
Genotype-Specific Recurrence Risks as Indicators of the Genetic Architecture of Complex Diseases
|
Slatkin, Montgomery
|
|
2008
|
83 |
1 |
p. 120-126
7 p.
|
artikel
|
| 8 |
Human Osteoclast-Poor Osteopetrosis with Hypogammaglobulinemia due to TNFRSF11A (RANK) Mutations
|
Guerrini, Matteo M.
|
|
2008
|
83 |
1 |
p. 64-76
13 p.
|
artikel
|
| 9 |
Infantile Spasms Is Associated with Deletion of the MAGI2 Gene on Chromosome 7q11.23-q21.11
|
Marshall, Christian R.
|
|
2008
|
83 |
1 |
p. 106-111
6 p.
|
artikel
|
| 10 |
Influence of Friedreich Ataxia GAA Noncoding Repeat Expansions on Pre-mRNA Processing
|
Baralle, Marco
|
|
2008
|
83 |
1 |
p. 77-88
12 p.
|
artikel
|
| 11 |
Long-Range LD Can Confound Genome Scans in Admixed Populations
|
Price, Alkes L.
|
|
2008
|
83 |
1 |
p. 132-135
4 p.
|
artikel
|
| 12 |
Loss of Function in Phenylketonuria Is Caused by Impaired Molecular Motions and Conformational Instability
|
Gersting, Søren W.
|
|
2008
|
83 |
1 |
p. 5-17
13 p.
|
artikel
|
| 13 |
Mitochondrial Hsp60 Chaperonopathy Causes an Autosomal-Recessive Neurodegenerative Disorder Linked to Brain Hypomyelination and Leukodystrophy
|
Magen, Daniella
|
|
2008
|
83 |
1 |
p. 30-42
13 p.
|
artikel
|
| 14 |
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 |
1 |
p. 99-105
7 p.
|
artikel
|
| 15 |
Personalized Genetics: A Responsible Approach
|
Stephan, Dietrich
|
|
2008
|
83 |
1 |
p. 130-
1 p.
|
artikel
|
| 16 |
Positive Selection in Alternatively Spliced Exons of Human Genes
|
Ramensky, Vasily E.
|
|
2008
|
83 |
1 |
p. 94-98
5 p.
|
artikel
|
| 17 |
Red-Green Color Vision Impairment in Duchenne Muscular Dystrophy
|
Costa, Marcelo Fernandes
|
|
2008
|
83 |
1 |
p. 148-149
2 p.
|
artikel
|
| 18 |
Reduced NODAL Signaling Strength via Mutation of Several Pathway Members Including FOXH1 Is Linked to Human Heart Defects and Holoprosencephaly
|
Roessler, Erich
|
|
2008
|
83 |
1 |
p. 18-29
12 p.
|
artikel
|
| 19 |
Reply to Hedrick
|
Kayser, Manfred
|
|
2008
|
83 |
1 |
p. 140-142
3 p.
|
artikel
|
| 20 |
Reply to Ho and Endicott
|
Fagundes, Nelson J.R.
|
|
2008
|
83 |
1 |
p. 146-147
2 p.
|
artikel
|
| 21 |
Reply to Stephan et al.
|
Janssens, A. Cecile J.W.
|
|
2008
|
83 |
1 |
p. 131-
1 p.
|
artikel
|
| 22 |
Response to Martignoni et al.
|
Mannan, Ashraf U.
|
|
2008
|
83 |
1 |
p. 128-130
3 p.
|
artikel
|
| 23 |
Response to Price et al.
|
Tang, Hua
|
|
2008
|
83 |
1 |
p. 135-139
5 p.
|
artikel
|
| 24 |
The Crucial Role of Calibration in Molecular Date Estimates for the Peopling of the Americas
|
Ho, Simon Y.W.
|
|
2008
|
83 |
1 |
p. 142-146
5 p.
|
artikel
|
| 25 |
The Role of ZFYVE27/Protrudin in Hereditary Spastic Paraplegia
|
Martignoni, Monica
|
|
2008
|
83 |
1 |
p. 127-128
2 p.
|
artikel
|
| 26 |
This Month in Genetics
|
Garber, Kathryn B.
|
|
2008
|
83 |
1 |
p. 3-4
2 p.
|
artikel
|
| 27 |
This Month in The Journal
|
Williamson, Robin E.
|
|
2008
|
83 |
1 |
p. 1-2
2 p.
|
artikel
|
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