| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A genetic variant in COL11A1 is functionally associated with lumbar disc herniation in Chinese population
|
Liu, Wenjun
|
|
2017
|
96 |
6 |
p. 867-872
|
artikel
|
| 2 |
Analysis of two susceptibility SNPs in HLA region and evidence of interaction between rs6457617 in HLA-DQB1 and HLA-DRB1*04 locus on Tunisian rheumatoid arthritis
|
Achour, Yosser
|
|
2017
|
96 |
6 |
p. 911-918
|
artikel
|
| 3 |
A novel contiguous deletion involving $$\varvec{NDP},$$NDP,MAOB and EFHC2 gene in a patient with familial Norrie disease: bilateral blindness and leucocoria without other deficits
|
Jia, Bei
|
|
2017
|
96 |
6 |
p. 1015-1020
|
artikel
|
| 4 |
A novel missense mutation of $$\textit{ADAR1}$$ADAR1 gene in a Chinese family leading to dyschromatosis symmetrica hereditaria and literature review
|
Liu, Shuai-Mei
|
|
2017
|
96 |
6 |
p. 1021-1026
|
artikel
|
| 5 |
Association of lactase 13910 C/T polymorphism with bone mineral density and fracture risk: a meta-analysis
|
Wu, Yougen
|
|
2017
|
96 |
6 |
p. 993-1003
|
artikel
|
| 6 |
Dominance effects estimation of TLR4 and CACNA2D1 genes for health and production traits using logistic regression
|
Bagheri, Masoumeh
|
|
2017
|
96 |
6 |
p. 1027-1031
|
artikel
|
| 7 |
Drosophila pallidosa: whether a separate species or a light form of D. ananassae
|
Singh, B. N.
|
|
2017
|
96 |
6 |
p. 1053-1059
|
artikel
|
| 8 |
Ellis–van Creveld syndrome and profound deafness resulted by sequence variants in the EVC / EVC2 and TMC1 genes
|
Umair, Muhammad
|
|
2017
|
96 |
6 |
p. 1005-1014
|
artikel
|
| 9 |
From the editor’s desk
|
|
|
2017
|
96 |
6 |
p. 865
|
artikel
|
| 10 |
Genetic analysis of 55 northern Vietnamese patients with Wilson disease: seven novel mutations in ATP7B
|
Pham, Le Anh Tuan
|
|
2017
|
96 |
6 |
p. 933-939
|
artikel
|
| 11 |
Genetic diversity, phylogeographic structure and effect of selection at the mitochondrial hypervariable region of Nigerian chicken populations
|
Ajibike, Abdulhakeem B.
|
|
2017
|
96 |
6 |
p. 959-968
|
artikel
|
| 12 |
Genetic variability and structure of an isolated population of Ambystoma altamirani, a mole salamander that lives in the mountains of one of the largest urban areas in the world
|
Heredia-Bobadilla, Rosa-Laura
|
|
2017
|
96 |
6 |
p. 873-883
|
artikel
|
| 13 |
Genetic variants influencing lipid levels and risk of dyslipidemia in Chinese population
|
Luo, Huaichao
|
|
2017
|
96 |
6 |
p. 985-992
|
artikel
|
| 14 |
Genome-based exome sequencing analysis identifies GYG1, DIS3L and DDRGK1 are associated with myocardial infarction in Koreans
|
Lee, Ji-Young
|
|
2017
|
96 |
6 |
p. 1041-1046
|
artikel
|
| 15 |
Glutathione S-transferase P1 gene polymorphisms and susceptibility to coronary artery disease in a subgroup of north Indian population
|
Bhat, M. A.
|
|
2017
|
96 |
6 |
p. 927-932
|
artikel
|
| 16 |
Identification and association of novel lncRNA pouMU1 gene mutations with chicken performance traits
|
Ren, Tuanhui
|
|
2017
|
96 |
6 |
p. 941-950
|
artikel
|
| 17 |
Identification of housekeeping genes as references for quantitative real-time RT-PCR analysis in Misgurnus anguillicaudatus
|
Xia, Xiaohua
|
|
2017
|
96 |
6 |
p. 895-904
|
artikel
|
| 18 |
Illumina-based de novo transcriptome sequencing and analysis of Chinese forest musk deer
|
Xu, Zhongxian
|
|
2017
|
96 |
6 |
p. 1033-1040
|
artikel
|
| 19 |
Influence of thiopurine methyltransferase gene polymorphism on Egyptian children with acute lymphoblastic leukaemia
|
Tantawy, Azza A. G.
|
|
2017
|
96 |
6 |
p. 905-910
|
artikel
|
| 20 |
Mapping of Id locus for dermal shank melanin in a Chinese indigenous chicken breed
|
Xu, Jiguo
|
|
2017
|
96 |
6 |
p. 977-983
|
artikel
|
| 21 |
Marker-assisted pyramiding of Thinopyrum-derived leaf rust resistance genes Lr19 and Lr24 in bread wheat variety HD2733
|
Singh, Mona
|
|
2017
|
96 |
6 |
p. 951-957
|
artikel
|
| 22 |
Mutational screening of PKD2 gene in the north Indian polycystic kidney disease patients revealed 28 genetic variations
|
Raj, Sonam
|
|
2017
|
96 |
6 |
p. 885-893
|
artikel
|
| 23 |
Neuro-fuzzy model of homocysteine metabolism
|
Naushad, Shaik Mohammad
|
|
2017
|
96 |
6 |
p. 919-926
|
artikel
|
| 24 |
The connexin 46 mutant (V44M) impairs gap junction function causing congenital cataract
|
Chen, Lijuan
|
|
2017
|
96 |
6 |
p. 969-976
|
artikel
|
| 25 |
Venous thromboembolism associated with protein S deficiency due to $$\hbox {Arg}451^{*}$$Arg451∗ mutation in PROS1 gene: a case report and a literature review
|
Wypasek, Ewa
|
|
2017
|
96 |
6 |
p. 1047-1051
|
artikel
|
Tijdschrift beschrijving