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Morris-Rosendahl, DJ
70
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Online (69)
Print (1)
Mediatypes
Books (1)
Articles (Online) (61)
Bookchapter (Online) (1)
OpenAccess-fulltext (7)
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german (1)
english (63)
Sorted by: Relevance
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?
1
Refining the phenotype of α-1a Tubulin (TUBA1A) mutation in..:
Morris-Rosendahl, DJ
;
Najm, J
;
Lachmeijer, AMA
...
Clinical Genetics. 74 (2008) 5 - p. 425-433 , 2008
Link:
https://doi.org/10.1111/..
?
2
PPA2-associated sudden cardiac death: extending the clinica..:
Guimier, A
;
Achleitner, MT
;
De Bellaing, AM
...
Genetics in Medicine. , 2021
Link:
http://hdl.handle.net/10..
?
3
PPA2-associated sudden cardiac death: extending the clinica..:
Guimier, A
;
Achleitner, MT
;
de Bellaing, AM
...
issn:1098-3600. , 2021
Link:
http://hdl.handle.net/11..
?
4
CardioClassifier: disease- and gene-specific computational ..:
Whiffin, N
;
Walsh, R
;
Govind, R
...
Genetics in medicine : official journal of the American College of Medical Genetics, 2018, 20 (10), pp. 1246 - 1254. , 2019
Link:
https://repository.icr.a..
?
5
De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy wi..:
Wallmeier, J
;
Frank, D
;
Shoemark, A
...
https://discovery.ucl.ac.uk/id/eprint/10085532/5/Mitchison_De%20Novo%20Mutations%20in%20FOXJ1%20Result_AAM.pdf. , 2019
Link:
https://discovery.ucl.ac..
?
6
CardioClassifier: disease- and gene-specific computational ..:
Whiffin, N
;
Walsh, R
;
Govind, R
...
https://discovery.ucl.ac.uk/id/eprint/10065557/1/gim.2017.258.pdf. , 2018
Link:
https://discovery.ucl.ac..
?
7
CardioClassifier – demonstrating the power of disease- and ..:
Whiffin, N
;
Walsh, R
;
Govind, R
...
https://discovery.ucl.ac.uk/id/eprint/10065760/7/Ahmad_180109.full.pdf. , 2017
Link:
https://discovery.ucl.ac..
?
8
What Next-Generation Sequencing (NGS) technology has enable..:
Morris-Rosendahl, DJ
;
Kaindl, A
Molecular and Cellular Probes. , 2015
Link:
http://hdl.handle.net/10..
?
9
Combined approaches, including long-read sequencing, addres..:
Fleming, Andrew
;
Galey, Miranda
;
Briggs, Lizi
...
European Journal of Human Genetics. , 2024
Link:
https://doi.org/10.1038/..
?
10
A novel variant in PTPN11, c.1277A>G p.(His426Arg), in a..:
Kuo, Olivia
;
Molloy, Kevin
;
Sabir, Ataf
...
Clinical and Experimental Dermatology. , 2024
Link:
https://doi.org/10.1093/..
?
11
EMQN: Recommendations for genetic testing in inherited card..:
Hayesmoore, Jesse B.
;
Bhuiyan, Zahurul A.
;
Coviello, Domenico A.
...
European Journal of Human Genetics. 31 (2023) 9 - p. 1003-1009 , 2023
Link:
https://doi.org/10.1038/..
?
12
The genetic basis of thoracic aortic disease: The future of..:
Salmasi, M Yousuf
;
Alwis, Shehani
;
Cyclewala, Shabnam
...
Hellenic Journal of Cardiology. 69 (2023) - p. 41-50 , 2023
Link:
https://doi.org/10.1016/..
?
13
Clinical and Neurophysiologic Phenotypes in Neonates WithBR..:
Carapancea, Evelina
;
Cornet, Marie-Coralie
;
Milh, Mathieu
...
Neurology. 100 (2023) 12 - p. , 2023
Link:
https://doi.org/10.1212/..
?
14
Prediction of next generation sequencing test failure in lu..:
Zhang, Yu Zhi
;
Sherlock, Stuart
;
MacMahon, Suzanne
...
Lung Cancer. 178 (2023) - p. S1-S2 , 2023
Link:
https://doi.org/10.1016/..
?
15
Type II Endoleaks and Culprit Vessels: Will 4D MRI Change t..:
Hanna, Lydia
;
Gibbs, Richard G.J.
;
Athanasiou, Thanos
...
European Journal of Vascular and Endovascular Surgery. 66 (2023) 1 - p. 148 , 2023
Link:
https://doi.org/10.1016/..
1-15