nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Association analysis of TNFRSF1B polymorphisms with type 2 diabetes and its related traits in North India
|
Tabassum, Rubina |
|
2009 |
2 |
3-4 |
p. 93-100 |
artikel |
2 |
Association analysis of TNFRSF1B polymorphisms with type 2 diabetes and its related traits in North India
|
Tabassum, Rubina |
|
|
2 |
3-4 |
p. 93-100 |
artikel |
3 |
Bioinformatics and statistical genomics
|
|
|
2009 |
2 |
3-4 |
p. 217-240 |
artikel |
4 |
Bioinformatics and statistical genomics
|
|
|
2009 |
2 |
3-4 |
p. 159-161 |
artikel |
5 |
Chemical genomics and molecular medicine
|
|
|
2009 |
2 |
3-4 |
p. 213-215 |
artikel |
6 |
Chemical genomics and molecular medicine
|
|
|
2009 |
2 |
3-4 |
p. 427-433 |
artikel |
7 |
Computational biology and structural proteomics
|
|
|
2009 |
2 |
3-4 |
p. 295-302 |
artikel |
8 |
Computational biology and structural proteomics
|
|
|
2009 |
2 |
3-4 |
p. 177-179 |
artikel |
9 |
David N. Cooper and Hildegard Kehrer-Sawatzki (eds): Handbook of Human Molecular Evolution
|
Kumar, Dhavendra |
|
2009 |
2 |
3-4 |
p. 127 |
artikel |
10 |
David N. Cooper and Hildegard Kehrer-Sawatzki (eds): Handbook of Human Molecular Evolution
|
Kumar, Dhavendra |
|
|
2 |
3-4 |
p. 127 |
artikel |
11 |
Disease proteomics
|
|
|
2009 |
2 |
3-4 |
p. 285-294 |
artikel |
12 |
Disease proteomics
|
|
|
2009 |
2 |
3-4 |
p. 173-175 |
artikel |
13 |
Disorders of the genome architecture: a review
|
Kumar, Dhavendra |
|
2009 |
2 |
3-4 |
p. 69-76 |
artikel |
14 |
Disorders of the genome architecture: a review
|
Kumar, Dhavendra |
|
|
2 |
3-4 |
p. 69-76 |
artikel |
15 |
Epigenomics
|
|
|
2009 |
2 |
3-4 |
p. 331-339 |
artikel |
16 |
Epigenomics
|
|
|
2009 |
2 |
3-4 |
p. 185-187 |
artikel |
17 |
Genes, chromosomes and disease
|
|
|
2009 |
2 |
3-4 |
p. 193-195 |
artikel |
18 |
Genes, chromosomes and disease
|
|
|
2009 |
2 |
3-4 |
p. 351-380 |
artikel |
19 |
Genome variation, diversity and evolution
|
|
|
2009 |
2 |
3-4 |
p. 253-271 |
artikel |
20 |
Genome variation, diversity and evolution
|
|
|
2009 |
2 |
3-4 |
p. 167-169 |
artikel |
21 |
Genomics of complex disorders I
|
|
|
2009 |
2 |
3-4 |
p. 303-330 |
artikel |
22 |
Genomics of complex disorders I
|
|
|
2009 |
2 |
3-4 |
p. 181-183 |
artikel |
23 |
Genomics of complex disorders II
|
|
|
2009 |
2 |
3-4 |
p. 389-400 |
artikel |
24 |
Genomics of complex disorders II
|
|
|
2009 |
2 |
3-4 |
p. 201-203 |
artikel |
25 |
Genomics of microbial pathogens and host–pathogen interactions
|
|
|
2009 |
2 |
3-4 |
p. 171-172 |
artikel |
26 |
Genomics of microbial pathogens and host–pathogen interactions
|
|
|
2009 |
2 |
3-4 |
p. 273-283 |
artikel |
27 |
Genomics of model organisms
|
|
|
2009 |
2 |
3-4 |
p. 415-425 |
artikel |
28 |
Genomics of model organisms
|
|
|
2009 |
2 |
3-4 |
p. 209-211 |
artikel |
29 |
HGM2008 cancer and epigenomics symposium abstracts
|
|
|
2009 |
2 |
3-4 |
p. 147-148 |
artikel |
30 |
HGM2008 complex disease genomics II symposium abstracts (neuropsychiatric and ocular disorders)
|
|
|
2009 |
2 |
3-4 |
p. 157-158 |
artikel |
31 |
HGM2008 complex disease genomics I symposium abstracts (diabetes, cardiovascular and respiratory diseases)
|
|
|
2009 |
2 |
3-4 |
p. 151-152 |
artikel |
32 |
HGM2008 ethics, culture and genomics symposium abstracts
|
|
|
2009 |
2 |
3-4 |
p. 153-154 |
artikel |
33 |
HGM2008 infectious diseases and metagenomics symposium abstracts
|
|
|
2009 |
2 |
3-4 |
p. 141-142 |
artikel |
34 |
HGM2008 new technologies: genome sequencing to molecular imaging symposium abstracts
|
|
|
2009 |
2 |
3-4 |
p. 149-150 |
artikel |
35 |
HGM2008 plenary abstracts: genome functions and systems biology
|
|
|
2009 |
2 |
3-4 |
p. 137-138 |
artikel |
36 |
HGM2008 plenary abstracts: genome informatics to genome biology
|
|
|
2009 |
2 |
3-4 |
p. 135-136 |
artikel |
37 |
HGM2008 plenary abstracts: genomics and the future of medicine
|
|
|
2009 |
2 |
3-4 |
p. 131-132 |
artikel |
38 |
HGM2008 plenary abstracts: landscape of genomic variation
|
|
|
2009 |
2 |
3-4 |
p. 133 |
artikel |
39 |
HGM 2008 population genetics and natural selection in man symposium abstracts
|
|
|
2009 |
2 |
3-4 |
p. 155-156 |
artikel |
40 |
HGM 2008 regulatory variation and non-coding DNA sequences symposium abstracts
|
|
|
2009 |
2 |
3-4 |
p. 143-144 |
artikel |
41 |
HGM2008 special plenary abstracts
|
|
|
2009 |
2 |
3-4 |
p. 139-140 |
artikel |
42 |
HGM2008 structural proteomics symposium abstracts
|
|
|
2009 |
2 |
3-4 |
p. 145-146 |
artikel |
43 |
High dose Losartan and ACE gene polymorphism in IgA nephritis
|
Woo, Keng-Thye |
|
2009 |
2 |
3-4 |
p. 83-91 |
artikel |
44 |
High dose Losartan and ACE gene polymorphism in IgA nephritis
|
Woo, Keng-Thye |
|
|
2 |
3-4 |
p. 83-91 |
artikel |
45 |
HUGO 20th anniversary lecture
|
|
|
2009 |
2 |
3-4 |
p. 129 |
artikel |
46 |
Identification of gene biomarkers for respiratory syncytial virus infection in a bronchial epithelial cell line
|
Huang, Yuh-Chin T. |
|
2009 |
2 |
3-4 |
p. 113-125 |
artikel |
47 |
In silico investigations on functional and haplotype tag SNPs associated with congenital long QT syndromes (LQTSs)
|
Sudandiradoss, C. |
|
2009 |
2 |
3-4 |
p. 55-67 |
artikel |
48 |
In silico investigations on functional and haplotype tag SNPs associated with congenital long QT syndromes (LQTSs)
|
Sudandiradoss, C. |
|
|
2 |
3-4 |
p. 55-67 |
artikel |
49 |
Karma, reincarnation, and medicine: Hindu perspectives on biomedical research
|
Hutchinson, Janis Faye |
|
2009 |
2 |
3-4 |
p. 107-111 |
artikel |
50 |
Late posters
|
|
|
2009 |
2 |
3-4 |
p. 435-438 |
artikel |
51 |
Micro RNA and non-coding DNA and repeats
|
|
|
2009 |
2 |
3-4 |
p. 401-413 |
artikel |
52 |
Micro RNA and non-coding DNA and repeats
|
|
|
2009 |
2 |
3-4 |
p. 205-207 |
artikel |
53 |
Pharmacogenetics education in British medical schools
|
Higgs, Jenny E. |
|
2009 |
2 |
3-4 |
p. 101-105 |
artikel |
54 |
Pharmacogenetics education in British medical schools
|
Higgs, Jenny E. |
|
|
2 |
3-4 |
p. 101-105 |
artikel |
55 |
Pharmacogenomics and toxicogenomics
|
|
|
2009 |
2 |
3-4 |
p. 189-191 |
artikel |
56 |
Pharmacogenomics and toxicogenomics
|
|
|
2009 |
2 |
3-4 |
p. 341-350 |
artikel |
57 |
Single gene disorders
|
|
|
2009 |
2 |
3-4 |
p. 163-165 |
artikel |
58 |
Single gene disorders
|
|
|
2009 |
2 |
3-4 |
p. 241-252 |
artikel |
59 |
Technology developments and applications
|
|
|
2009 |
2 |
3-4 |
p. 197-199 |
artikel |
60 |
Technology developments and applications
|
|
|
2009 |
2 |
3-4 |
p. 381-388 |
artikel |
61 |
Two sisters with Rett syndrome and non-identical paternally-derived microdeletions in the MECP2 gene
|
Rosser, Lyndon G. |
|
2008 |
2 |
3-4 |
p. 77-81 |
artikel |
62 |
Two sisters with Rett syndrome and non-identical paternally-derived microdeletions in the MECP2 gene
|
Rosser, Lyndon G. |
|
|
2 |
3-4 |
p. 77-81 |
artikel |