E-LIB Suche - Ergebnisse für: Alina C. Hilger

1

Familial congenital lower urinary tract obstruction (LUTO) ..:

Ebach, Fabian ; Wagner, Pauline ; Stein, Raimund...
Health Science Reports. 7 (2024) 3 - p. , 2024

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

2

PKD1L1 Is Involved in Congenital Chylothorax:

Whitchurch, Jonathan B. ; Schneider, Sophia ; Hilger, Alina C....
Cells. 13 (2024) 2 - p. 149 , 2024

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

3

Long-Term Experience of Arterio-Venous Fistula Surgery in C..:

Almási-Sperling, Veronika ; Gall, Christine ; Haney, Briain...
Journal of Clinical Medicine. 13 (2024) 12 - p. 3577 , 2024

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

4

Exome Survey and Candidate Gene Re-Sequencing Identifies No..:

Köllges, Ricarda ; Stegmann, Jil ; Schneider, Sophia...
Biomolecules. 13 (2023) 7 - p. 1117 , 2023

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

5

Modelling human lower urinary tract malformations in zebraf..:

Kolvenbach, Caroline M. ; Dworschak, Gabriel C. ; Rieke, Johanna M....
Molecular and Cellular Pediatrics. 10 (2023) 1 - p. , 2023

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

6

Resequencing of VEGFR3 pathway genes implicate GJC2 and FLT..:

Schneider, Sophia ; Köllges, Ricarda ; Stegmann, Jil D....
American Journal of Medical Genetics Part A. 188 (2022) 5 - p. 1607-1611 , 2022

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

7

Re‐sequencing of candidate genes FOXF1, HSPA6, HAAO, and KY..:

Thiem, Corina E. ; Stegmann, Jil D. ; Hilger, Alina C....
Birth Defects Research. 114 (2022) 10 - p. 478-486 , 2022

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

8

A genome-wide association study with tissue transcriptomics..:

Mingardo, Enrico ; Beaman, Glenda ; Grote, Philip...
Communications Biology. 5 (2022) 1 - p. , 2022

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

9

Diverse ancestry whole-genome sequencing association study ..:

Chan, Melanie MY ; Sadeghi-Alavijeh, Omid ; Lopes, Filipa M...
eLife. 11 (2022) - p. , 2022

Link: https://doi.org/10.7554/..

10

X-linked variations inSHROOM4are implicated in congenital a..:

Kolvenbach, Caroline M ; Felger, Tim ; Schierbaum, Luca...
Journal of Medical Genetics. 60 (2022) 6 - p. 587-596 , 2022

Link: https://doi.org/10.1136/..

11

Definition, diagnosis and clinical management of non-obstru..:

Kohl, Stefan ; Avni, Fred E ; Boor, Peter...
Nephrology Dialysis Transplantation. 37 (2022) 12 - p. 2351-2362 , 2022

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

12

Genome-wide association study in patients with posterior ur..:

van der Zanden, Loes F. M. ; Maj, Carlo ; Borisov, Oleg...
Frontiers in Pediatrics. 10 (2022) - p. , 2022

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

13

Exome sequencing in individuals with cardiovascular lateral..:

Breuer, Katinka ; Riedhammer, Korbinian M. ; Müller, Nicole...
European Journal of Human Genetics. 30 (2022) 8 - p. 946-954 , 2022

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

14

Exome survey of individuals affected by VATER/VACTERL with ..:

Kolvenbach, Caroline M. ; van der Ven, Amelie T. ; Kause, Franziska...
American Journal of Medical Genetics Part A. 185 (2021) 12 - p. 3784-3792 , 2021

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

15

Genome-Wide Survey for Microdeletions or -Duplications in 1..:

Schierbaum, Luca M. ; Schneider, Sophia ; Herms, Stefan...
Genes. 12 (2021) 9 - p. 1449 , 2021

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