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Adenaeuer, Anke
14
results:
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1
Severe high-molecular-weight kininogen deficiency: clinical..:
Adenaeuer, Anke
;
Barco, Stefano
;
Trinchero, Alice
...
https://boris.unibe.ch/177969/. , 2023
Link:
https://boris.unibe.ch/1..
?
2
Hereditary spherocytosis : can next-generation sequencing o..:
Häuser, Friederike
;
Rossmann, Heidi
;
Adenaeuer, Anke
...
http://doi.org/10.25358/openscience-9760. , 2023
Link:
https://openscience.ub.u..
?
3
Hereditary Spherocytosis: Can Next-Generation Sequencing of..:
Häuser, Friederike
;
Rossmann, Heidi
;
Adenaeuer, Anke
...
https://boris.unibe.ch/190092/. , 2023
Link:
https://boris.unibe.ch/1..
?
4
Second MAFA Variant Causing a Phosphorylation Defect in the..:
Fottner, Christian
;
Sollfrank, Stefanie
;
Ghiasi, Mursal
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8997416/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
5
Second MAFA variant causing a phosphorylation defect in the..:
Fottner, Christian
;
Sollfrank, Stefanie
;
Ghiasi, Mursal
...
http://doi.org/10.25358/openscience-7026. , 2022
Link:
https://openscience.ub.u..
?
6
c.451dupT in KLKB1 is common in Nigerians, confirming a hig..:
Adenaeuer, Anke
;
Ezigbo, D. Eyiuche
;
Nazir, Hanan Fawzy
...
http://doi.org/10.25358/openscience-6169. , 2021
Link:
https://openscience.ub.u..
?
7
Severe plasma prekallikrein deficiency: Clinical characteri..:
Barco, Stefano
;
Sollfrank, Stefanie
;
Trinchero, Alice
...
https://boris.unibe.ch/149801/. , 2020
Link:
https://boris.unibe.ch/1..
?
8
Severe plasma prekallikrein deficiency : clinical character..:
Barco, Stefano
;
Sollfrank, Stefanie
;
Trinchero, Alice
...
http://doi.org/10.25358/openscience-6292. , 2020
Link:
https://openscience.ub.u..
?
9
Severe plasma prekallikrein deficiency: clinical characteri..:
Barco, Stefano
;
Sollfrank, Stefanie
;
Trinchero, Alice
...
https://freidok.uni-freiburg.de/data/167091. , 2020
Link:
https://freidok.uni-frei..
?
10
Hereditary Spherocytosis: Can Next-Generation Sequencing of..:
Friederike Häuser
;
Heidi Rossmann
;
Anke Adenaeuer
...
https://www.mdpi.com/1422-0067/24/23/17021. , 2023
Link:
https://doi.org/10.3390/..
?
11
Second MAFA Variant Causing a Phosphorylation Defect in the..:
Christian Fottner
;
Stefanie Sollfrank
;
Mursal Ghiasi
...
Cancer Therapy. , 2022
Link:
https://doi.org/10.3390/..
?
12
Novel GATA1 Variant Causing a Bleeding Phenotype Associated..:
Kerstin Jurk
;
Anke Adenaeuer
;
Stefanie Sollfrank
...
Cellular Pathology. , 2022
Link:
https://doi.org/10.3390/..
?
13
Second MAFA Variant Causing a Phosphorylation Defect in the..:
Christian Fottner
;
Stefanie Sollfrank
;
Mursal Ghiasi
...
https://www.mdpi.com/2072-6694/14/7/1798. , 2022
Link:
https://doi.org/10.3390/..
?
14
Novel GATA1 Variant Causing a Bleeding Phenotype Associated..:
Kerstin Jurk
;
Anke Adenaeuer
;
Stefanie Sollfrank
...
https://www.mdpi.com/2073-4409/11/19/3071. , 2022
Link:
https://doi.org/10.3390/..
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