| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acknowledgement to Referees
|
|
|
2017
|
21 |
6 |
p. 581-585
|
artikel
|
| 2 |
Acknowledgement to Referees
|
|
|
|
21 |
6 |
p. 581-585
|
artikel
|
| 3 |
Are the Origins of Precision Medicine Found in the Corpus Hippocraticum?
|
Konstantinidou, Meropi K.
|
|
2017
|
21 |
6 |
p. 601-606
|
artikel
|
| 4 |
Are the Origins of Precision Medicine Found in the Corpus Hippocraticum?
|
Konstantinidou, Meropi K.
|
|
|
21 |
6 |
p. 601-606
|
artikel
|
| 5 |
Authors’ Reply to Uguen: “Comparison of Five Different Assays for the Detection of BRAF Mutations in Formalin-Fixed Paraffin Embedded Tissues of Patients with Metastatic Melanoma”
|
Harlé, Alexandre
|
|
2017
|
21 |
6 |
p. 695-696
|
artikel
|
| 6 |
Authors’ Reply to Uguen: “Comparison of Five Different Assays for the Detection of BRAF Mutations in Formalin-Fixed Paraffin Embedded Tissues of Patients with Metastatic Melanoma”
|
Harlé, Alexandre
|
|
|
21 |
6 |
p. 695-696
|
artikel
|
| 7 |
Circulating mRNA in Maternal Plasma at the Second Trimester of Pregnancy: A Possible Screening Tool for Cardiac Conotruncal and Left Ventricular Outflow Tract Abnormalities
|
Contro, Elena
|
|
2017
|
21 |
6 |
p. 653-661
|
artikel
|
| 8 |
Circulating mRNA in Maternal Plasma at the Second Trimester of Pregnancy: A Possible Screening Tool for Cardiac Conotruncal and Left Ventricular Outflow Tract Abnormalities
|
Contro, Elena
|
|
|
21 |
6 |
p. 653-661
|
artikel
|
| 9 |
Comment on: “Comparison of Five Different Assays for the Detection of BRAF Mutations in Formalin-Fixed Paraffin Embedded Tissues of Patients with Metastatic Melanoma”
|
Uguen, Arnaud
|
|
2017
|
21 |
6 |
p. 693-694
|
artikel
|
| 10 |
Comment on: “Comparison of Five Different Assays for the Detection of BRAF Mutations in Formalin-Fixed Paraffin Embedded Tissues of Patients with Metastatic Melanoma”
|
Uguen, Arnaud
|
|
|
21 |
6 |
p. 693-694
|
artikel
|
| 11 |
Development of CYP21A2 Genotyping Assay for the Diagnosis of Congenital Adrenal Hyperplasia
|
Prado, Mayara Jorgens
|
|
2017
|
21 |
6 |
p. 663-675
|
artikel
|
| 12 |
Development of CYP21A2 Genotyping Assay for the Diagnosis of Congenital Adrenal Hyperplasia
|
Prado, Mayara Jorgens
|
|
|
21 |
6 |
p. 663-675
|
artikel
|
| 13 |
Genetic Counseling in Primary Immunodeficiency Disorders: An Emerging Experience in Egypt
|
El Hawary, Rabab E.
|
|
2017
|
21 |
6 |
p. 677-684
|
artikel
|
| 14 |
Genetic Counseling in Primary Immunodeficiency Disorders: An Emerging Experience in Egypt
|
El Hawary, Rabab E.
|
|
|
21 |
6 |
p. 677-684
|
artikel
|
| 15 |
Increased Sensitivity of Diagnostic Mutation Detection by Re-analysis Incorporating Local Reassembly of Sequence Reads
|
Watson, Christopher M.
|
|
2017
|
21 |
6 |
p. 685-692
|
artikel
|
| 16 |
Increased Sensitivity of Diagnostic Mutation Detection by Re-analysis Incorporating Local Reassembly of Sequence Reads
|
Watson, Christopher M.
|
|
|
21 |
6 |
p. 685-692
|
artikel
|
| 17 |
Medullary Thyroid Cancer: Clinical Characteristics and New Insights into Therapeutic Strategies Targeting Tyrosine Kinases
|
Rajabi, Sadegh
|
|
2017
|
21 |
6 |
p. 607-620
|
artikel
|
| 18 |
Medullary Thyroid Cancer: Clinical Characteristics and New Insights into Therapeutic Strategies Targeting Tyrosine Kinases
|
Rajabi, Sadegh
|
|
|
21 |
6 |
p. 607-620
|
artikel
|
| 19 |
MicroRNA-21 in Skin Fibrosis: Potential for Diagnosis and Treatment
|
Li, Yan
|
|
2017
|
21 |
6 |
p. 633-642
|
artikel
|
| 20 |
MicroRNA-21 in Skin Fibrosis: Potential for Diagnosis and Treatment
|
Li, Yan
|
|
|
21 |
6 |
p. 633-642
|
artikel
|
| 21 |
Pharmacogenetics and Pharmacogenomics of Targeted Therapeutics in Chronic Myeloid Leukemia
|
Nath, Aritro
|
|
2017
|
21 |
6 |
p. 621-631
|
artikel
|
| 22 |
Pharmacogenetics and Pharmacogenomics of Targeted Therapeutics in Chronic Myeloid Leukemia
|
Nath, Aritro
|
|
|
21 |
6 |
p. 621-631
|
artikel
|
| 23 |
Prospective Turkish Cohort Study to Investigate the Frequency of Niemann-Pick Disease Type C Mutations in Consanguineous Families with at Least One Homozygous Family Member
|
Topçu, Meral
|
|
2017
|
21 |
6 |
p. 643-651
|
artikel
|
| 24 |
Prospective Turkish Cohort Study to Investigate the Frequency of Niemann-Pick Disease Type C Mutations in Consanguineous Families with at Least One Homozygous Family Member
|
Topçu, Meral
|
|
|
21 |
6 |
p. 643-651
|
artikel
|
| 25 |
The Role of BEAMing and Digital PCR for Multiplexed Analysis in Molecular Oncology in the Era of Next-Generation Sequencing
|
Denis, Jérôme Alexandre
|
|
2017
|
21 |
6 |
p. 587-600
|
artikel
|
| 26 |
The Role of BEAMing and Digital PCR for Multiplexed Analysis in Molecular Oncology in the Era of Next-Generation Sequencing
|
Denis, Jérôme Alexandre
|
|
|
21 |
6 |
p. 587-600
|
artikel
|
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