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Fagerberg, Christina
204
results:
Search for persons
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Format
Online (204)
Mediatypes
Articles (Online) (52)
OpenAccess-fulltext (152)
Languages
english (192)
danish (3)
Sorted by: Relevance
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?
1
Expansion of the neurodevelopmental phenotype of individual..:
Paulet, Alix
;
Bennett-Ness, Cavan
;
Ageorges, Faustine
...
European Journal of Human Genetics. , 2024
Link:
https://doi.org/10.1038/..
?
2
Reclassification of an FBN1 variant emphasizes the importan..:
Lildballe, Dorte L.
;
Markholt, Sara
;
Lyngholm, Christina Daugaard
...
American Journal of Medical Genetics Part A. , 2024
Link:
https://doi.org/10.1002/..
?
3
Variants in the WDR44 WD40-repeat domain cause a spectrum o..:
Accogli, Andrea
;
Shakya, Saurabh
;
Yang, Taewoo
...
Nature Communications. 15 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1038/..
?
4
Correction: Expansion of the neurodevelopmental phenotype o..:
Paulet, Alix
;
Bennett-Ness, Cavan
;
Ageorges, Faustine
...
European Journal of Human Genetics. , 2024
Link:
https://doi.org/10.1038/..
?
5
P428: De novo truncating variants in ZNF865: A putative cau..:
Bradbrook, Sam
;
Graham, Gail
;
Carter, Melissa
...
Genetics in Medicine Open. 2 (2024) - p. 101322 , 2024
Link:
https://doi.org/10.1016/..
?
6
A Novel CDC42 Variant with Impaired Thymopoiesis, IL-7R Sig..:
Assing, Kristian
;
Jørgensen, Sofie E.
;
Sandgaard, Katrine S.
...
Journal of Clinical Immunology. 43 (2023) 8 - p. 1927-1940 , 2023
Link:
https://doi.org/10.1007/..
?
7
Comprehensive prenatal diagnostics: Exome versus genome seq..:
Miceikaite, Ieva
;
Fagerberg, Christina
;
Brasch‐Andersen, Charlotte
...
Prenatal Diagnosis. 43 (2023) 9 - p. 1132-1141 , 2023
Link:
https://doi.org/10.1002/..
?
8
Genotype-Phenotype Comparison in POGZ-Related Neurodevelopm..:
Nagy, Dóra
;
Verheyen, Sarah
;
Wigby, Kristen M.
...
Genes. 13 (2022) 1 - p. 154 , 2022
Link:
https://doi.org/10.3390/..
?
9
Expanding the genotype and phenotype spectrum of SYT1-assoc..:
Melland, Holly
;
Bumbak, Fabian
;
Kolesnik-Taylor, Anna
...
Genetics in Medicine. 24 (2022) 4 - p. 880-893 , 2022
Link:
https://doi.org/10.1016/..
?
10
Variants in ADD1 cause intellectual disability, corpus call..:
Qi, Cai
;
Feng, Irena
;
Costa, Ana Rita
...
Genetics in Medicine. 24 (2022) 2 - p. 319-331 , 2022
Link:
https://doi.org/10.1016/..
?
11
National data on the early clinical use of non‐invasive pre..:
Lund, Ida C. B.
;
Petersen, Olav B.
;
Becher, Naja H.
...
Acta Obstetricia et Gynecologica Scandinavica. 100 (2021) 5 - p. 884-892 , 2021
Link:
https://doi.org/10.1111/..
?
12
Total number of reads affects the accuracy of fetal fractio..:
Miceikaitė, Ieva
;
Brasch‐Andersen, Charlotte
;
Fagerberg, Christina
.
Molecular Genetics & Genomic Medicine. 9 (2021) 4 - p. , 2021
Link:
https://doi.org/10.1002/..
?
13
Trisomy 8 mosaicism in the placenta: A Danish cohort study ..:
Thomsen, Simon Horsholt
;
Lund, Ida Charlotte Bay
;
Fagerberg, Christina
...
Prenatal Diagnosis. 41 (2020) 4 - p. 409-421 , 2020
Link:
https://doi.org/10.1002/..
?
14
A novel PDGFRB sequence variant in a family with a mild for..:
Mathorne, Stine Westergaard
;
Sørensen, Kristina
;
Fagerberg, Christina
..
BMC Neurology. 19 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1186/..
?
15
Deletions and loss-of-function variants in TP63 associated ..:
Khandelwal, Kriti D.
;
van den Boogaard, Marie-José H.
;
Mehrem, Sarah L.
...
European Journal of Human Genetics. 27 (2019) 7 - p. 1101-1112 , 2019
Link:
https://doi.org/10.1038/..
1-15