A rapid method for detection of five known mutations associated with aminoglycoside-induced deafness.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 2, doi. 10.1186/1471-2350-10-2
- Publication type:
- Article
Works matching IS 14712350 AND DT 2009 AND VI 10
Results: 151
1
2
Differentially expressed alternatively spliced genes in MalignantPleural Mesothelioma identified using massively paralleltranscriptome sequencing.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 149, doi. 10.1186/1471-2350-10-149
- Publication type:
- Article
3
Evaluating NAT2PRED for inferring the individual acetylationstatus from unphased genotype data.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 148, doi. 10.1186/1471-2350-10-148
- Publication type:
- Article
4
Association of DRD4 uVNTR and TP53 codon 72 polymorphismswith schizophrenia: a case-control study.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 147, doi. 10.1186/1471-2350-10-147
- Publication type:
- Article
5
Genome screen in familial intracranial aneurysm.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 3, doi. 10.1186/1471-2350-10-3
- Publication type:
- Article
6
Characterisation of CYP2C8, CYP2C9 and CYP2C19 polymorphismsin a Ghanaian population.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 124, doi. 10.1186/1471-2350-10-124
- Publication type:
- Article
7
Confirmation of the genetic association of CTLA4 and PTPN22 withANCA-associated vasculitis.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 121, doi. 10.1186/1471-2350-10-121
- Publication type:
- Article
8
DYRK1A genetic variants are not linked to Alzheimer's disease in a Spanish case-control cohort.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 129, doi. 10.1186/1471-2350-10-129
- Publication type:
- Article
9
Association between CYP19 gene SNP rs2414096 Polymorphism and polycystic ovary syndrome in Chinese women.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 139, doi. 10.1186/1471-2350-10-139
- Publication type:
- Article
10
Mitochondrial DNA haplogroup T is associated with coronary artery disease and diabetic retinopathy: a case control study.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 35, doi. 10.1186/1471-2350-10-35
- Publication type:
- Article
11
Lack of association between PRNP 1368 polymorphism and Alzheimer's disease or vascular dementia.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 32, doi. 10.1186/1471-2350-10-32
- Publication type:
- Article
12
SLC6A3 and body mass index in the Prostate, Lung, Colorectal and Ovarian Cancer Screening Trial.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 9, doi. 10.1186/1471-2350-10-9
- Publication type:
- Article
13
An open access database of genome-wide association results.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 6, doi. 10.1186/1471-2350-10-6
- Publication type:
- Article
14
Genetic and other factors determining mannose-binding lectin levels in American Indians: the Strong Heart Study.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 5, doi. 10.1186/1471-2350-10-5
- Publication type:
- Article
15
Common genetic variants of the ion channel transient receptor potential membrane melastatin 6 and 7 (TRPM6 and TRPM7), magnesium intake, and risk of type 2 diabetes in women.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 4, doi. 10.1186/1471-2350-10-4
- Publication type:
- Article
16
PRNP variation in UK sporadic and variant Creutzfeldt Jakobdisease highlights genetic risk factors and a novel non-synonymouspolymorphism.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 146, doi. 10.1186/1471-2350-10-146
- Publication type:
- Article
17
PLCLI rs75954I2 variation is not associated with hip bone sizevariation in postmenopausal Danish women.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 145, doi. 10.1186/1471-2350-10-145
- Publication type:
- Article
18
BAC array CGH in patients with Velocardiofacial syndrome-likefeatures reveals genomic aberrations on chromosome regionIq2I.I.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 144, doi. 10.1186/1471-2350-10-144
- Publication type:
- Article
19
A tagging SNP in INSIG2 is associated with obesity-relatedphenotypes among Samoans.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 143, doi. 10.1186/1471-2350-10-143
- Publication type:
- Article
20
Use of supplementary phenotype to identify additional rheumatoidarthritis loci in a linkage analysis of 342 UK affected sibling pairfamilies.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 142, doi. 10.1186/1471-2350-10-142
- Publication type:
- Article
21
Association of a functional microsatellite within intron I of theBMP5 gene with susceptibility to osteoarthritis.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 141, doi. 10.1186/1471-2350-10-141
- Publication type:
- Article
22
Melusin gene (ITGBIBP2) nucleotide variations study inhypertensive and cardiopathic patients.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 140, doi. 10.1186/1471-2350-10-140
- Publication type:
- Article
23
Association between CYPI9 gene SNP rs24I4096 Polymorphismand polycystic ovary syndrome in Chinese women.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 1
- Publication type:
- Article
24
Innate immunity in ocular Chlamydia trachomatis infection:contribution of IL8 and CSF2 gene variants to risk of trachomatousscarring in Gambians.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 138, doi. 10.1186/1471-2350-10-138
- Publication type:
- Article
25
Association of a de novo 16q copy number variant with a phenotypethat overlaps with Lenz microphthalmia and Townes-Brockssyndromes.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 137, doi. 10.1186/1471-2350-10-137
- Publication type:
- Article
26
Reduced transcription of TCOFI in adult cells of Treacher Collinssyndrome patients.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 136, doi. 10.1186/1471-2350-10-136
- Publication type:
- Article
27
STK39 polymorphisms and blood pressure: an association study inBritish Caucasians and assessment of cis-acting influences on geneexpression.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 135, doi. 10.1186/1471-2350-10-135
- Publication type:
- Article
28
The neck-region polymorphism of DC-SIGNR in peri-centenarianfrom Han Chinese Population.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 134, doi. 10.1186/1471-2350-10-134
- Publication type:
- Article
29
Evidence for an association of HLA-DRBI*15 and DRBI*09 withleprosy and the impact of DRBI *09 on disease onset in a ChineseHan population.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 133
- Publication type:
- Article
30
Association of ADAM33 gene polymorphisms with COPD in anortheastern Chinese population.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 132, doi. 10.1186/1471-2350-10-132
- Publication type:
- Article
31
The common FTO variant rs9939609 is not associated with BMI in alongitudinal study on a cohort of Swedish men born 1920-1924.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 131, doi. 10.1186/1471-2350-10-131
- Publication type:
- Article
32
Genetic variation of NEDD4L is associated with essentialhypertension in female Kazakh general population: a case-controlstudy.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 130, doi. 10.1186/1471-2350-10-130
- Publication type:
- Article
33
DYRKIA genetic variants are not linked to Alzheimer's disease in aSpanish case-control cohort.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 500
- Publication type:
- Article
34
A pooling-based genome-wide analysis identifies new potentialcandidate genes for atopy in the European Community RespiratoryHealth Survey (ECRHS).
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 128, doi. 10.1186/1471-2350-10-128
- Publication type:
- Article
35
Relationship of circulating cell-free DNA levels to cell-free fetal DNA levels, clinical characteristics and laboratory parameters in preeclampsia.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 120, doi. 10.1186/1471-2350-10-120
- Publication type:
- Article
36
The rs I 990760 polymorphism within the IFIHI locus is notassociated with Graves' disease, Hashimoto's thyroiditis andAddison's disease.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 126, doi. 10.1186/1471-2350-10-126
- Publication type:
- Article
37
Association of vitamin D receptor polymorphisms with the risk ofprostate cancer in the Han population of Southern China.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 125, doi. 10.1186/1471-2350-10-125
- Publication type:
- Article
38
Analyses of associations between three positionally cloned asthmacandidate genes and asthma or asthma-related phenotypes in aChinese population.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 123, doi. 10.1186/1471-2350-10-123
- Publication type:
- Article
39
Further analysis of previously implicated linkage regions for Alzheimer's disease in affected relative pairs.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 122, doi. 10.1186/1471-2350-10-122
- Publication type:
- Article
40
Power of multifactor dimensionality reduction and penalizedlogistic regression for detecting gene-gene Interactionin a case-control study.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 127, doi. 10.1186/1471-2350-10-127
- Publication type:
- Article
41
A novel study of Copy Number Variations in Hirschsprung disease using the Multiple Ligation-dependent Probe Amplification (MLPA) technique.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 119, doi. 10.1186/1471-2350-10-119
- Publication type:
- Article
42
HECTD2, a candidate susceptibility gene for Alzheimer's disease on 10q.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 90, doi. 10.1186/1471-2350-10-90
- Publication type:
- Article
43
Suggestive linkage detected for blood pressure related traits on 2q and 22q in the population on the Samoan islands.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 107, doi. 10.1186/1471-2350-10-107
- Publication type:
- Article
44
Emilin 1 gene and essential hypertension: a two-stage association study in northern Han Chinese population.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 118, doi. 10.1186/1471-2350-10-118
- Publication type:
- Article
45
Genetic variation in the NBS1, MRE11, RAD50 and BLM genes and susceptibility to non-Hodgkin lymphoma.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 117, doi. 10.1186/1471-2350-10-117
- Publication type:
- Article
46
Molecular analysis of T-B-NK<sup>+</sup> severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 116, doi. 10.1186/1471-2350-10-116
- Publication type:
- Article
47
PIN1 gene variants in Alzheimer's disease.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 115, doi. 10.1186/1471-2350-10-115
- Publication type:
- Article
48
Voltage-dependent anion channel (VDAC) is involved in apoptosis of cell lines carrying the mitochondrial DNA mutation.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 114, doi. 10.1186/1471-2350-10-114
- Publication type:
- Article
49
ALDH1A2 (RALDH2) genetic variation in human congenital heart disease.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 113, doi. 10.1186/1471-2350-10-113
- Publication type:
- Article
50
Do the mutations of C1GALT1C1 gene play important roles in the genetic susceptibility to Chinese IgA nephropathy?
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 101, doi. 10.1186/1471-2350-10-101
- Publication type:
- Article