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                             27 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A Genome-wide Survey of the Prevalence and Evolutionary Forces Acting on Human Nonsense SNPs Yngvadottir, Bryndis
2009
84 2 p. 224-234
11 p.
artikel
2 A Homozygous Mutation in ADAMTSL4 Causes Autosomal-Recessive Isolated Ectopia Lentis Ahram, Dina
2009
84 2 p. 274-278
5 p.
artikel
3 Allan Award Lecture: On Jumping Fields and “Jumping Genes” Kazazian Jr., Haig H.
2009
84 2 p. 105-114
10 p.
artikel
4 A Missense Mutation in CASK Causes FG Syndrome in an Italian Family Piluso, Giulio
2009
84 2 p. 162-177
16 p.
artikel
5 A Multiplex Human Syndrome Implicates a Key Role for Intestinal Cell Kinase in Development of Central Nervous, Skeletal, and Endocrine Systems Lahiry, Piya
2009
84 2 p. 134-147
14 p.
artikel
6 A Testing Framework for Identifying Susceptibility Genes in the Presence of Epistasis Millstein, Joshua
2009
84 2 p. 301-
1 p.
artikel
7 A Unified Approach to Genotype Imputation and Haplotype-Phase Inference for Large Data Sets of Trios and Unrelated Individuals Browning, Brian L.
2009
84 2 p. 210-223
14 p.
artikel
8 Awards and Addresses Summary 2009
84 2 p. 101-102
2 p.
artikel
9 A Whole-Genome Scan and Fine-Mapping Linkage Study of Auditory-Visual Synesthesia Reveals Evidence of Linkage to Chromosomes 2q24, 5q33, 6p12, and 12p12 Asher, Julian E.
2009
84 2 p. 279-285
7 p.
artikel
10 Common Variation in the β-Carotene 15,15′-Monooxygenase 1 Gene Affects Circulating Levels of Carotenoids: A Genome-wide Association Study Ferrucci, Luigi
2009
84 2 p. 123-133
11 p.
artikel
11 Genome-wide Linkage Scan Reveals Three Putative Breast-Cancer-Susceptibility Loci Rosa-Rosa, Juan Manuel
2009
84 2 p. 115-122
8 p.
artikel
12 Genotype-Imputation Accuracy across Worldwide Human Populations Huang, Lucy
2009
84 2 p. 235-250
16 p.
artikel
13 Inferential Genotyping of Y Chromosomes in Latter-Day Saints Founders and Comparison to Utah Samples in the HapMap Project Gitschier, Jane
2009
84 2 p. 251-258
8 p.
artikel
14 Is the Tail-Strength Measure More Powerful in Tests of Genetic Association? Han, Shizhong
2009
84 2 p. 295-298
4 p.
artikel
15 Mutations in CNNM4 Cause Jalili Syndrome, Consisting of Autosomal-Recessive Cone-Rod Dystrophy and Amelogenesis Imperfecta Parry, David A.
2009
84 2 p. 266-273
8 p.
artikel
16 Mutations in CNNM4 Cause Recessive Cone-Rod Dystrophy with Amelogenesis Imperfecta Polok, Bozena
2009
84 2 p. 259-265
7 p.
artikel
17 Mutations in Radial Spoke Head Protein Genes RSPH9 and RSPH4A Cause Primary Ciliary Dyskinesia with Central-Microtubular-Pair Abnormalities Castleman, Victoria H.
2009
84 2 p. 197-209
13 p.
artikel
18 Mutations in SPINT2 Cause a Syndromic Form of Congenital Sodium Diarrhea Heinz-Erian, Peter
2009
84 2 p. 188-196
9 p.
artikel
19 Mutations in STIL, Encoding a Pericentriolar and Centrosomal Protein, Cause Primary Microcephaly Kumar, Arun
2009
84 2 p. 286-290
5 p.
artikel
20 Population Analysis of Large Copy Number Variants and Hotspots of Human Genetic Disease Itsara, Andy
2009
84 2 p. 148-161
14 p.
artikel
21 Response to Zang et al. and Han et al. Wang, Jian
2009
84 2 p. 298-300
3 p.
artikel
22 Searching for Genotype-Phenotype Structure: Using Hierarchical Log-Linear Models in Crohn Disease Chapman, Juliet M.
2009
84 2 p. 178-187
10 p.
artikel
23 Tail Strength to Combine Two p Values: Their Correlation Cannot Be Ignored Zang, Yong
2009
84 2 p. 291-295
5 p.
artikel
24 TFAP2A Mutations Result in Branchio-Oculo-Facial Syndrome Milunsky, Jeff M.
2009
84 2 p. 301-
1 p.
artikel
25 This Month in Genetics Garber, Kathryn B.
2009
84 2 p. 99-100
2 p.
artikel
26 This Month in The Journal Bungartz, Kathryn D.
2009
84 2 p. 97-98
2 p.
artikel
27 William Allan Award Introduction: Haig H. Kazazian, Jr. Antonarakis, Stylianos E.
2009
84 2 p. 103-104
2 p.
artikel
                             27 gevonden resultaten
 
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