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de Haan, Amber
45
results:
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Online (45)
Mediatypes
Articles (Online) (10)
OpenAccess-fulltext (35)
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1
Novel MUC1 variant identified by massively parallel sequenc..:
de Haan, Amber
;
van Eerde, Albertien M.
;
Eijgelsheim, Mark
...
Kidney International. 103 (2023) 5 - p. 986-989 , 2023
Link:
https://doi.org/10.1016/..
?
2
Diagnostic yield of massively parallel sequencing in patien..:
de Haan, Amber
;
Eijgelsheim, Mark
;
Vogt, Liffert
...
BMJ Open. 12 (2022) 4 - p. e057829 , 2022
Link:
https://doi.org/10.1136/..
?
3
Genetic Determinants of Serum Calcification Propensity and ..:
de Haan, Amber
;
Ahmadizar, Fariba
;
van der Most, Peter J.
...
Frontiers in Cardiovascular Medicine. 8 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
4
Fabry disease with atypical phenotype identified by massive..:
de Haan, Amber
;
Morel, Chantal F
;
Eijgelsheim, Mark
...
Clinical Kidney Journal. 16 (2022) 4 - p. 722-726 , 2022
Link:
https://doi.org/10.1093/..
?
5
MO034: Novel MUC1 variant identified by massively parallel ..:
de Haan, Amber
;
Eijgelsheim, Mark
;
Rump, Patrick
...
Nephrology Dialysis Transplantation. 37 (2022) Supplement_3 - p. , 2022
Link:
https://doi.org/10.1093/..
?
6
A mutation update for theFLNCgene in myopathies and cardiom..:
Verdonschot, Job A. J.
;
Vanhoutte, Els K.
;
Claes, Godelieve R. F.
...
Human Mutation. 41 (2020) 6 - p. 1091-1111 , 2020
Link:
https://doi.org/10.1002/..
?
7
Diagnostic Yield of Next-Generation Sequencing in Patients ..:
de Haan, Amber
;
Eijgelsheim, Mark
;
Vogt, Liffert
..
Frontiers in Genetics. 10 (2019) - p. , 2019
Link:
https://doi.org/10.3389/..
?
8
Genetic testing in adult-onset chronic kidney disease: unra..:
de Haan, Amber
https://research.rug.nl/en/publications/11e84c40-2bfa-461d-bc0a-529bea47fe2b. , 2024
Link:
https://hdl.handle.net/1..
?
9
Novel MUC1 variant identified by massively parallel sequenc..:
de Haan, Amber
;
van Eerde, Albertien M
;
Eijgelsheim, Mark
...
https://research.rug.nl/en/publications/5313e589-62f4-4e1d-894d-5d98b91c5e20. , 2023
Link:
https://hdl.handle.net/1..
?
10
Novel MUC1 variant identified by massively parallel sequenc..:
de Haan, Amber
;
van Eerde, Albertien M
;
Eijgelsheim, Mark
...
0085-2538. , 2023
Link:
https://dspace.library.u..
?
11
Fabry disease with atypical phenotype identified by massive..:
de Haan, Amber
;
Morel, Chantal F
;
Eijgelsheim, Mark
...
https://research.rug.nl/en/publications/fead96b0-0272-48b7-98d9-9d5d652095ff. , 2023
Link:
https://hdl.handle.net/1..
?
12
Diagnostic yield of massively parallel sequencing in patien..:
de Haan, Amber
;
Eijgelsheim, Mark
;
Vogt, Liffert
...
2044-6055. , 2022
Link:
https://dspace.library.u..
?
13
Genetic Determinants of Serum Calcification Propensity and ..:
de Haan, Amber
;
Ahmadizar, Fariba
;
van der Most, Peter J
...
https://research.rug.nl/en/publications/166dbb5d-1f11-4574-bf96-15215030ded0. , 2022
Link:
https://hdl.handle.net/1..
?
14
Diagnostic yield of massively parallel sequencing in patien..:
de Haan, Amber
;
Eijgelsheim, Mark
;
Vogt, Liffert
...
https://research.rug.nl/en/publications/e2a24c99-5b0b-44e5-a8ad-dfc0421a0fd1. , 2022
Link:
https://hdl.handle.net/1..
?
15
Genetic Determinants of Serum Calcification Propensity and ..:
de Haan, Amber
;
Ahmadizar, Fariba
;
van der Most, Peter J
...
https://pure.eur.nl/en/publications/587a79d3-9683-44bb-84d2-568fa9a877f6. , 2021
Link:
https://pure.eur.nl/en/p..
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