E-LIB Suche - Ergebnisse für: Bartram, Claus R.

1

Genetic Variation in ABCC4 and CFTR and Acute Pancreatitis ..:

Bartram, Thies ; Schütte, Peter ; Möricke, Anja...
Journal of Clinical Medicine. 10 (2021) 21 - p. 4815 , 2021

Link: https://doi.org/10.3390/..

2

The Frog Xenopus as a Model to Study Joubert Syndrome: The ..:

Ott, Tim ; Kaufmann, Lilian ; Granzow, Martin...
Frontiers in Physiology. 10 (2019) - p. , 2019

Link: https://doi.org/10.3389/..

3

Identification of four novel associations for B-cell acute ..:

Vijayakrishnan, Jayaram ; Qian, Maoxiang ; Studd, James B....
Nature Communications. 10 (2019) 1 - p. , 2019

Link: https://doi.org/10.1038/..

4

Breast cancer risk in BRCA1/2 mutation carriers and noncarr..:

Engel, Christoph ; Fischer, Christine ; Zachariae, Silke...
International Journal of Cancer. 146 (2019) 4 - p. 999-1009 , 2019

Link: https://doi.org/10.1002/..

5

Large scale multifactorial likelihood quantitative analysis..:

Parsons, Michael T. ; Tudini, Emma ; Li, Hongyan...
Human Mutation. 40 (2019) 9 - p. 1557-1578 , 2019

Link: https://doi.org/10.1002/..

6

Single CpG hypermethylation, allele methylation errors, and..:

Böck, Julia ; Appenzeller, Silke ; Haertle, Larissa...
International Journal of Cancer. 143 (2018) 6 - p. 1416-1425 , 2018

Link: https://doi.org/10.1002/..

7

Validation of Minimal Residual Disease as Surrogate Endpoin..:

Galimberti, Stefania ; Devidas, Meenakshi ; Lucenti, Ausiliatrice...
JNCI Cancer Spectrum. 2 (2018) 4 - p. , 2018

Link: https://doi.org/10.1093/..

8

Prevalence of pathogenic BRCA1/2 germline mutations among 8..:

on behalf of the German Consortium for Hereditary Breast and Ovarian Cancer (GC-HBOC) ; Engel, Christoph ; Rhiem, Kerstin...
BMC Cancer. 18 (2018) 1 - p. , 2018

Link: https://doi.org/10.1186/..

9

The association between breast cancer and S100P methylation..:

Yang, Rongxi ; Stöcker, Sarah ; Schott, Sarah...
Carcinogenesis. 38 (2017) 3 - p. 312-320 , 2017

Link: https://doi.org/10.1093/..

10

Impact of clinical exomes in neurodevelopmental and neurome..:

Evers, Christina ; Staufner, Christian ; Granzow, Martin...
Molecular Genetics and Metabolism. 121 (2017) 4 - p. 297-307 , 2017

Link: https://doi.org/10.1016/..

11

Diagnosis of CoPAN by whole exome sequencing: Waking up a s..:

Evers, Christina ; Seitz, Angelika ; Assmann, Birgit...
American Journal of Medical Genetics Part A. 173 (2017) 7 - p. 1878-1886 , 2017

Link: https://doi.org/10.1002/..

12

DDX3X mutations in two girls with a phenotype overlapping T..:

Dikow, Nicola ; Granzow, Martin ; Graul‐Neumann, Luitgard M....
American Journal of Medical Genetics Part A. 173 (2017) 5 - p. 1369-1373 , 2017

Link: https://doi.org/10.1002/..

13

Exome sequencing reveals a novel CWF19L1 mutation associate..:

Evers, Christina ; Kaufmann, Lilian ; Seitz, Angelika...
American Journal of Medical Genetics Part A. 170 (2016) 6 - p. 1502-1509 , 2016

Link: https://doi.org/10.1002/..

14

Next-generation personalised medicine for high-risk paediat..:

Worst, Barbara C. ; van Tilburg, Cornelis M. ; Balasubramanian, Gnana Prakash...
European Journal of Cancer. 65 (2016) - p. 91-101 , 2016

Link: https://doi.org/10.1016/..

15

DNA methylation array analysis identifies breast cancer ass..:

Tang, Qiuqiong ; Holland-Letz, Tim ; Slynko, Alla...
Oncotarget. 7 (2016) 39 - p. 64191-64202 , 2016

Link: https://doi.org/10.18632..