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Ćomić, Jasmina
24
results:
Search for persons
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Format
Online (24)
Mediatypes
Articles (Online) (8)
OpenAccess-fulltext (16)
Sorted by: Relevance
Sorted by: Year
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1
#1012 Lifetime risk of autosomal recessive kidney diseases ..:
Braunisch, Matthias
;
Großewinkelmann, Clara
;
Menke, Martin
...
Nephrology Dialysis Transplantation. 39 (2024) Supplement_1 - p. , 2024
Link:
https://doi.org/10.1093/..
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2
Implication of transcription factor FOXD2 dysfunction in sy..:
Riedhammer, Korbinian M.
;
Nguyen, Thanh-Minh T.
;
Koşukcu, Can
...
Kidney International. 105 (2024) 4 - p. 844-864 , 2024
Link:
https://doi.org/10.1016/..
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3
Is there a dominant‐negative effect in individuals with het..:
Riedhammer, Korbinian M.
;
Simmendinger, Hannes
;
Tasic, Velibor
...
Clinical Genetics. 105 (2024) 4 - p. 406-414 , 2024
Link:
https://doi.org/10.1111/..
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4
Exome sequencing in individuals with congenital anomalies o..:
Riedhammer, Korbinian M.
;
Ćomić, Jasmina
;
Tasic, Velibor
...
European Journal of Human Genetics. 31 (2023) 6 - p. 674-680 , 2023
Link:
https://doi.org/10.1038/..
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5
#4876 CLASSIFICATION OF BIOPSY FINDINGS IN INDIVIDUALS WITH..:
Zellner, Alicia
;
Schaaf, Christian
;
Buettner-Herold, Maike
...
Nephrology Dialysis Transplantation. 38 (2023) Supplement_1 - p. , 2023
Link:
https://doi.org/10.1093/..
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6
Renal X-inactivation in female individuals with X-linked Al..:
Günthner, Roman
;
Knipping, Lea
;
Jeruschke, Stefanie
...
Frontiers in Medicine. 9 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
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7
The multifaceted phenotypic and genotypic spectrum of type-..:
Ćomić, Jasmina
;
Riedhammer, Korbinian M.
;
Günthner, Roman
...
Frontiers in Medicine. 9 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
8
High detection rate for disease-causing variants in a cohor..:
Najafi, Maryam
;
Riedhammer, Korbinian M.
;
Rad, Aboulfazl
...
Frontiers in Pediatrics. 10 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
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9
Implication of FOXD2 dysfunction in syndromic congenital an..:
Riedhammer, Korbinian M
;
Nguyen, Thanh-Minh T
;
Koşukcu, Can
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055578/. , 2023
Link:
http://www.ncbi.nlm.nih...
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10
The multifaceted phenotypic and genotypic spectrum of type-..:
Ćomić, Jasmina
;
Riedhammer, Korbinian M
;
Günthner, Roman
...
https://resolver.sub.uni-goettingen.de/purl?gro-2/114576. , 2022
Link:
https://resolver.sub.uni..
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11
Renal X-inactivation in female individuals with X-linked Al..:
Günthner, Roman
;
Knipping, Lea
;
Jeruschke, Stefanie
...
2296-858X. , 2022
Link:
https://resolver.sub.uni..
?
12
The multifaceted phenotypic and genotypic spectrum of type-..:
Ćomić, Jasmina
;
Riedhammer, Korbinian M
;
Günthner, Roman
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9470833/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
13
Renal X-inactivation in female individuals with X-linked Al..:
Günthner, Roman
;
Knipping, Lea
;
Jeruschke, Stefanie
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9630586/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
14
High detection rate for disease-causing variants in a cohor..:
Najafi, Maryam
;
Riedhammer, Korbinian M
;
Rad, Aboulfazl
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9555279/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
15
High detection rate for disease-causing variants in a cohor..:
Najafi, Maryam
;
Riedhammer, Korbinian M
;
Rad, Aboulfazl
...
https://freidok.uni-freiburg.de/data/230450. , 2022
Link:
https://freidok.uni-frei..
1-15