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                             22 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Abraham's Children in the Genome Era: Major Jewish Diaspora Populations Comprise Distinct Genetic Clusters with Shared Middle Eastern Ancestry Atzmon, Gil
2010
86 6 p. 850-859
10 p.
artikel
2 A Definitive Haplotype Map as Determined by Genotyping Duplicated Haploid Genomes Finds a Predominant Haplotype Preference at Copy-Number Variation Events Kukita, Yoji
2010
86 6 p. 918-928
11 p.
artikel
3 Cranioectodermal Dysplasia, Sensenbrenner Syndrome, Is a Ciliopathy Caused by Mutations in the IFT122 Gene Walczak-Sztulpa, Joanna
2010
86 6 p. 949-956
8 p.
artikel
4 Dominant-Negative Mutations in α-II Spectrin Cause West Syndrome with Severe Cerebral Hypomyelination, Spastic Quadriplegia, and Developmental Delay Saitsu, Hirotomo
2010
86 6 p. 881-891
11 p.
artikel
5 Evolutionary and Functional Analysis of Celiac Risk Loci Reveals SH2B3 as a Protective Factor against Bacterial Infection Zhernakova, Alexandra
2010
86 6 p. 970-977
8 p.
artikel
6 Female-to-Male Breeding Ratio in Modern Humans—an Analysis Based on Historical Recombinations Labuda, Damian
2010
86 6 p. 982-
1 p.
artikel
7 GJC2 Missense Mutations Cause Human Lymphedema Ferrell, Robert E.
2010
86 6 p. 943-948
6 p.
artikel
8 Haploinsufficiency of TAB2 Causes Congenital Heart Defects in Humans Thienpont, Bernard
2010
86 6 p. 839-849
11 p.
artikel
9 Identification of a Kir3.4 Mutation in Congenital Long QT Syndrome Yang, Yanzong
2010
86 6 p. 872-880
9 p.
artikel
10 Insights into Colon Cancer Etiology via a Regularized Approach to Gene Set Analysis of GWAS Data Chen, Lin S.
2010
86 6 p. 860-871
12 p.
artikel
11 Loss-of-Function Mutations in HPSE2 Cause the Autosomal Recessive Urofacial Syndrome Pang, Junfeng
2010
86 6 p. 957-962
6 p.
artikel
12 Mechanisms for Nonrecurrent Genomic Rearrangements Associated with CMT1A or HNPP: Rare CNVs as a Cause for Missing Heritability Zhang, Feng
2010
86 6 p. 892-903
12 p.
artikel
13 Mutations in HPSE2 Cause Urofacial Syndrome Daly, Sarah B.
2010
86 6 p. 963-969
7 p.
artikel
14 Pooled Association Tests for Rare Variants in Exon-Resequencing Studies Price, Alkes L.
2010
86 6 p. 982-
1 p.
artikel
15 Pooled Association Tests for Rare Variants in Exon-Resequencing Studies Price, Alkes L.
2010
86 6 p. 832-838
7 p.
artikel
16 Powerful SNP-Set Analysis for Case-Control Genome-wide Association Studies Wu, Michael C.
2010
86 6 p. 929-942
14 p.
artikel
17 Principal-Component Analysis for Assessment of Population Stratification in Mitochondrial Medical Genetics Biffi, Alessandro
2010
86 6 p. 904-917
14 p.
artikel
18 Response to Lohmueller et al. Labuda, Damian
2010
86 6 p. 980-981
2 p.
artikel
19 Sex-Averaged Recombination and Mutation Rates on the X Chromosome: A Comment on Labuda et al. Lohmueller, Kirk E.
2010
86 6 p. 978-980
3 p.
artikel
20 The Woman Who Walked into the Sea: Huntington's and the Making of a Genetic Disease Uhlmann, Wendy R.
2010
86 6 p. 830-831
2 p.
artikel
21 This Month in Genetics Garber, Kathryn B.
2010
86 6 p. 827-829
3 p.
artikel
22 This Month in The Journal Bungartz, Kathryn D.
2010
86 6 p. 825-826
2 p.
artikel
                             22 gevonden resultaten
 
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