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                             17 gevonden resultaten
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
                             17 gevonden resultaten
 
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