nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A Commercial Real-Time PCR Kit Provides Greater Sensitivity than Direct Sequencing to Detect KRAS Mutations
|
Angulo, Bárbara |
|
2010 |
12 |
3 |
p. 292-299 8 p. |
artikel |
2 |
A Novel COL7A1 Gene Mutation in an Iranian Individual Suffering Dystrophic Epidermolysis Bullosa
|
Galehdari, Hamid |
|
2010 |
12 |
3 |
p. 377-379 3 p. |
artikel |
3 |
A Synonymous Mutation in the CFTR Gene Causes Aberrant Splicing in an Italian Patient Affected by a Mild Form of Cystic Fibrosis
|
Faa′, Valeria |
|
2010 |
12 |
3 |
p. 380-383 4 p. |
artikel |
4 |
Bead Array–Based microRNA Expression Profiling of Peripheral Blood and the Impact of Different RNA Isolation Approaches
|
Gaarz, Andrea |
|
2010 |
12 |
3 |
p. 335-344 10 p. |
artikel |
5 |
Combined Use of PCR-Based TCRG and TCRB Clonality Tests on Paraffin-Embedded Skin Tissue in the Differential Diagnosis of Mycosis Fungoides and Inflammatory Dermatoses
|
Zhang, Bing |
|
2010 |
12 |
3 |
p. 320-327 8 p. |
artikel |
6 |
Detection of Exon 12 Mutations in the JAK2 Gene
|
Laughlin, Todd S. |
|
2010 |
12 |
3 |
p. 278-282 5 p. |
artikel |
7 |
Development of a Diagnostic Microarray Assay to Assess the Risk of Recurrence of Prostate Cancer Based on PITX2 DNA Methylation
|
Schatz, Philipp |
|
2010 |
12 |
3 |
p. 345-353 9 p. |
artikel |
8 |
High Expression of Lymphocyte-Activation Gene 3 (LAG3) in Chronic Lymphocytic Leukemia Cells Is Associated with Unmutated Immunoglobulin Variable Heavy Chain Region (IGHV) Gene and Reduced Treatment-Free Survival
|
Kotaskova, Jana |
|
2010 |
12 |
3 |
p. 328-334 7 p. |
artikel |
9 |
Rapid and Reliable Detection of Glucose-6-Phosphate Dehydrogenase (G6PD) Gene Mutations in Han Chinese Using High-Resolution Melting Analysis
|
Yan, Jing-bin |
|
2010 |
12 |
3 |
p. 305-311 7 p. |
artikel |
10 |
Rapid Diagnosis of α-Thalassemia by Melting Curve Analysis
|
Munkongdee, Thongperm |
|
2010 |
12 |
3 |
p. 354-358 5 p. |
artikel |
11 |
Rapid Genetic Analysis of X-Linked Chronic Granulomatous Disease by High-Resolution Melting
|
Hill, Harry R. |
|
2010 |
12 |
3 |
p. 368-376 9 p. |
artikel |
12 |
Rare Sequence Variation in the Genome Flanking a Short Tandem Repeat Locus Can Lead to a Question of “Nonmaternity”
|
Deucher, Anne |
|
2010 |
12 |
3 |
p. 384-389 6 p. |
artikel |
13 |
SeqSharp
|
SenGupta, Dhruba J. |
|
2010 |
12 |
3 |
p. 272-277 6 p. |
artikel |
14 |
Serum DNA Motifs Predict Disease and Clinical Status in Multiple Sclerosis
|
Beck, Julia |
|
2010 |
12 |
3 |
p. 312-319 8 p. |
artikel |
15 |
Simultaneous Genotyping of GSTT1 and GSTM1 Null Polymorphisms by Melting Curve Analysis in Presence of SYBR Green I
|
Marín, Fátima |
|
2010 |
12 |
3 |
p. 300-304 5 p. |
artikel |
16 |
Surpassing Specificity Limits of Nucleic Acid Probes via Cooperativity
|
Satterfield, Brent C. |
|
2010 |
12 |
3 |
p. 359-367 9 p. |
artikel |
17 |
Towards Routine Screening of Rare Genetic Diseases
|
Stasia, Marie José |
|
2010 |
12 |
3 |
p. 269-271 3 p. |
artikel |
18 |
Validation and Comparison of Pharmacogenetics-Based Warfarin Dosing Algorithms for Application of Pharmacogenetic Testing
|
Roper, Nitin |
|
2010 |
12 |
3 |
p. 283-291 9 p. |
artikel |