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Paske, Iris te
51
results:
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Online (50)
Print (1)
Mediatypes
Books (1)
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Articles (Online) (23)
OpenAccess-fulltext (26)
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german (1)
english (50)
Sorted by: Relevance
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?
1
A Solve-RD ClinVar-based reanalysis of 1522 index cases fro..:
Denommé-Pichon, Anne-Sophie
;
Matalonga, Leslie
;
de Boer, Elke
...
https://doi.org/10.1016/j.gim.2023.100018. , 2023
Link:
http://orbilu.uni.lu/han..
?
2
Solving patients with rare diseases through programmatic re..:
Sommer, Anna Katharina
;
Paske, Iris Te
;
Dizjikan, Farid Yavari
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41431-021-00852-7. , 2021
Link:
https://hal.sorbonne-uni..
?
3
Solving patients with rare diseases through programmatic re..:
Matalonga, Leslie
;
Hernández-Ferrer, Carles
;
Piscia, Davide
...
http://shura.shu.ac.uk/29063/. , 2021
Link:
https://shura.shu.ac.uk/..
?
4
Solving patients with rare diseases through programmatic re..:
Sommer, Anna Katharina
;
Paske, Iris Te
;
Dizjikan, Farid Yavari
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41431-021-00852-7. , 2021
Link:
https://hal.sorbonne-uni..
?
5
Solving patients with rare diseases through programmatic re..:
Sommer, Anna Katharina
;
Paske, Iris Te
;
Dizjikan, Farid Yavari
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41431-021-00852-7. , 2021
Link:
https://hal.sorbonne-uni..
?
6
Solving patients with rare diseases through programmatic re..:
Sommer, Anna Katharina
;
Paske, Iris Te
;
Dizjikan, Farid Yavari
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41431-021-00852-7. , 2021
Link:
https://hal.sorbonne-uni..
?
7
Solving patients with rare diseases through programmatic re..:
Sommer, Anna Katharina
;
Paske, Iris te
;
Dizjikan, Farid Yavari
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41431-021-00852-7. , 2021
Link:
https://hal.sorbonne-uni..
?
8
Wnt genes in colonic polyposis predisposition:
Quintana, Isabel
;
Terradas, Mariona
;
Mur, Pilar
...
Genes & Diseases. 10 (2023) 3 - p. 753-757 , 2023
Link:
https://doi.org/10.1016/..
?
9
Combined loss of CDH1 and downstream regulatory sequences d..:
São José, Celina
;
Garcia-Pelaez, José
;
Ferreira, Marta
...
Gastric Cancer. 26 (2023) 5 - p. 653-666 , 2023
Link:
https://doi.org/10.1007/..
?
10
Correction: Mobile element insertions in rare diseases: a c..:
Wijngaard, Robin
;
Demidov, German
;
O'Gorman, Luke
...
European Journal of Human Genetics. , 2023
Link:
https://doi.org/10.1038/..
?
11
Mobile element insertions in rare diseases: a comparative b..:
Wijngaard, Robin
;
Demidov, German
;
O'Gorman, Luke
...
European Journal of Human Genetics. , 2023
Link:
https://doi.org/10.1038/..
?
12
Germline mutations inWNK2could be associated with serrated ..:
Soares de Lima, Yasmin
;
Arnau-Collell, Coral
;
Muñoz, Jenifer
...
Journal of Medical Genetics. 60 (2022) 6 - p. 557-567 , 2022
Link:
https://doi.org/10.1136/..
?
13
Noncoding Aberrations in Mismatch Repair Genes Underlie a S..:
Te Paske, Iris B.A.W.
;
Mensenkamp, Arjen R.
;
Neveling, Kornelia
...
Gastroenterology. 163 (2022) 6 - p. 1691-1694.e7 , 2022
Link:
https://doi.org/10.1053/..
?
14
Solving the genetic aetiology of hereditary gastrointestina..:
Sommer, Anna K.
;
te Paske, Iris B.A.W.
;
Garcia-Pelaez, José
...
European Journal of Medical Genetics. 65 (2022) 5 - p. 104475 , 2022
Link:
https://doi.org/10.1016/..
?
15
A mosaic PIK3CA variant in a young adult with diffuse gastr..:
te Paske, Iris B. A. W.
;
Garcia-Pelaez, José
;
Sommer, Anna K.
...
European Journal of Human Genetics. 29 (2021) 9 - p. 1354-1358 , 2021
Link:
https://doi.org/10.1038/..
1-15
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