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Doll, Julia
87
results:
english X
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Online (87)
Mediatypes
Articles (Online) (38)
Bookchapter (Online) (1)
OpenAccess-fulltext (48)
Sorted by: Relevance
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?
1
Epithelioid and spindle cell rhabdomyosarcoma with EWSR1::T..:
Haug, Lukas
;
Doll, Julia
;
Appenzeller, Silke
...
Pathology - Research and Practice. 249 (2023) - p. 154779 , 2023
Link:
https://doi.org/10.1016/..
?
2
mRNA Abundance of Neurogenic Factors Correlates with Hearin..:
Engert, Jonas
;
Doll, Julia
;
Vona, Barbara
...
Life. 13 (2023) 9 - p. 1858 , 2023
Link:
https://doi.org/10.3390/..
?
3
Unraveling the genetic complexities of combined retinal dys..:
Bahena, Paulina
;
Daftarian, Narsis
;
Maroofian, Reza
...
Human Genetics. 141 (2021) 3-4 - p. 785-803 , 2021
Link:
https://doi.org/10.1007/..
?
4
Genetic Spectrum of Syndromic and Non-Syndromic Hearing Los..:
Doll, Julia
;
Vona, Barbara
;
Schnapp, Linda
...
Genes. 11 (2020) 11 - p. 1329 , 2020
Link:
https://doi.org/10.3390/..
?
5
Non-syndromic hearing loss: clinical and diagnostic challen..:
Vona, Barbara
;
Doll, Julia
;
Hofrichter, Michaela A. H.
.
Medizinische Genetik. 32 (2020) 2 - p. 117-129 , 2020
Link:
https://doi.org/10.1515/..
?
6
Small fish, big prospects: using zebrafish to unravel the m..:
Vona, Barbara
;
Doll, Julia
;
Hofrichter, Michaela A.H.
..
Hearing Research. 397 (2020) - p. 107906 , 2020
Link:
https://doi.org/10.1016/..
?
7
A novel missense variant in MYO3A is associated with autoso..:
Doll, Julia
;
Hofrichter, Michaela A. H.
;
Bahena, Paulina
...
Molecular Genetics & Genomic Medicine. 8 (2020) 8 - p. , 2020
Link:
https://doi.org/10.1002/..
?
8
Novel Loss-of-Function Variants in CDC14A are Associated wi..:
Doll, Julia
;
Kolb, Susanne
;
Schnapp, Linda
...
International Journal of Molecular Sciences. 21 (2020) 1 - p. 311 , 2020
Link:
https://doi.org/10.3390/..
?
9
Exome-wide copy number variation analysis identifies a COL9..:
Hofrichter, Michaela A.H.
;
Doll, Julia
;
Habibi, Haleh
...
European Journal of Medical Genetics. 62 (2019) 10 - p. 103724 , 2019
Link:
https://doi.org/10.1016/..
?
10
The conserved p.Arg108 residue in S1PR2 (DFNB68) is fundame..:
Hofrichter, Michaela A. H.
;
Mojarad, Majid
;
Doll, Julia
...
BMC Medical Genetics. 19 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1186/..
?
11
The CAPOS mutation in ATP1A3 alters Na/K-ATPase function an..:
Tranebjærg, Lisbeth
;
Strenzke, Nicola
;
Lindholm, Sture
...
Human Genetics. 137 (2018) 2 - p. 111-127 , 2018
Link:
https://doi.org/10.1007/..
?
12
Correction to: The CAPOS mutation in ATP1A3 alters Na/K-ATP..:
Tranebjærg, Lisbeth
;
Strenzke, Nicola
;
Lindholm, Sture
...
Human Genetics. 137 (2018) 3 - p. 279-280 , 2018
Link:
https://doi.org/10.1007/..
?
13
mRNA Abundance of Neurogenic Factors Correlates with Hearin..:
Engert, Jonas
;
Doll, Julia
;
Vona, Barbara
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10532994/. , 2023
Link:
http://www.ncbi.nlm.nih...
?
14
mRNA Abundance of Neurogenic Factors Correlates with Hearin..:
Engert, Jonas
;
Doll, Julia
;
Vona, Barbara
...
https://resolver.sub.uni-goettingen.de/purl?gro-2/133140. , 2023
Link:
https://resolver.sub.uni..
?
15
Unraveling the genetic complexities of combined retinal dys..:
Bahena, Paulina
;
Daftarian, Narsis
;
Maroofian, Reza
...
https://opus.bibliothek.uni-wuerzburg.de/frontdoor/index/index/docId/26775. , 2022
Link:
https://opus.bibliothek...
1-15