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Varon, Raymonda
232
results:
Format
Online (231)
Print (1)
Mediatypes
Articles (Online) (45)
Articles (Print) (1)
OpenAccess-fulltext (186)
Sorted by: Relevance
Sorted by: Year
?
1
Transmission ratio distortion of mutations in the master re..:
Neitzel, Heidemarie
;
Varon, Raymonda
;
Chughtai, Sana
...
Human Genetics. 141 (2022) 11 - p. 1785-1794 , 2022
Link:
https://doi.org/10.1007/..
?
2
The NBN founder mutation—Evidence for a country specific di..:
Chrzanowska, Krystyna H.
;
Seemanova, Eva
;
Varon, Raymonda
...
Cancer Reports. 6 (2022) 2 - p. , 2022
Link:
https://doi.org/10.1002/..
?
3
Investigating the effects of additional truncating variants..:
Sepahi, Ilnaz
;
Faust, Ulrike
;
Sturm, Marc
...
BMC Cancer. 19 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1186/..
?
4
Yeast XRS2 and human NBN gene: Experimental evidence for ho..:
Demuth, Ilja
;
Krebs, Simon K.
;
Dutrannoy, Véronique
...
PLOS ONE. 13 (2018) 11 - p. e0207315 , 2018
Link:
https://doi.org/10.1371/..
?
5
The Slavic NBN Founder Mutation: A Role for Reproductive Fi..:
Seemanova, Eva
;
Varon, Raymonda
;
Vejvalka, Jan
...
PLOS ONE. 11 (2016) 12 - p. e0167984 , 2016
Link:
https://doi.org/10.1371/..
?
6
QF-PCR as a molecular-based method for autosomal aneuploidi..:
Moftah, Reham
;
Marzouk, Salah
;
El-Kaffash, Dalal
...
Advances in Reproductive Sciences. 1 (2013) 3 - p. 21-28 , 2013
Link:
https://doi.org/10.4236/..
?
7
A 17‐year‐old adolescent with anorexia and gait abnormaliti..:
Meyer, Sascha
;
Gortner, Ludwig
;
Varon, Raymonda
...
Acta Paediatrica. 101 (2012) 9 - p. , 2012
Link:
https://doi.org/10.1111/..
?
8
New mutations in the ATM gene and clinical data of 25 AT pa..:
Demuth, Ilja
;
Dutrannoy, Véronique
;
Marques Jr, Wilson
...
neurogenetics. 12 (2011) 4 - p. 273-282 , 2011
Link:
https://doi.org/10.1007/..
?
9
Fatal Cardiac Arrhythmia and Long-QT Syndrome in a New Form..:
Rajab, Anna
;
Straub, Volker
;
McCann, Liza J.
...
PLoS Genetics. 6 (2010) 3 - p. e1000874 , 2010
Link:
https://doi.org/10.1371/..
?
10
Genetic variants within miR-126 and miR-335 are not associa..:
Yang, Rongxi
;
Dick, Michelle
;
Marme, Frederik
...
Breast Cancer Research and Treatment. 127 (2010) 2 - p. 549-554 , 2010
Link:
https://doi.org/10.1007/..
?
11
Clinical variability and novel mutations in the NHEJ1 gene ..:
Dutrannoy, Véronique
;
Demuth, Ilja
;
Baumann, Ulrich
...
Human Mutation. 31 (2010) 9 - p. 1059-1068 , 2010
Link:
https://doi.org/10.1002/..
?
12
Human RAD50 deficiency in a Nijmegen breakage syndrome-like..:
, In:
American journal of human genetics / American Society of Human Genetics
Waltes, Regina
;
Gatei, Magtouf
;
Kijas, Amanda W.
.... (2009) 5 - p. 605-616
Copies:
Zentrale:
z hbi 820 jc/81;
Zentrale:Magazin Zs
fb 2581
?
13
A genetic variant in the pre-miR-27a oncogene is associated..:
Yang, Rongxi
;
Schlehe, Bettina
;
Hemminki, Kari
...
Breast Cancer Research and Treatment. 121 (2009) 3 - p. 693-702 , 2009
Link:
https://doi.org/10.1007/..
?
14
Clinical variability in distal spinal muscular atrophy type..:
Guenther, Ulf-Peter
;
Handoko, Lusy
;
Varon, Raymonda
...
Journal of Molecular Medicine. 87 (2008) 1 - p. 31-41 , 2008
Link:
https://doi.org/10.1007/..
?
15
Nijmegen Breakage Syndrome mutations and risk of breast can..:
Bogdanova, Natalia
;
Feshchenko, Sergei
;
Schürmann, Peter
...
International Journal of Cancer. 122 (2007) 4 - p. 802-806 , 2007
Link:
https://doi.org/10.1002/..
1-15