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Alexandrou, Angelos
71
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Online (71)
Mediatypes
Articles (Online) (37)
OpenAccess-fulltext (34)
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1
A novel large intragenic DPYD deletion causing dihydropyrim..:
Malekkou, Anna
;
Tomazou, Marios
;
Mavrikiou, Gavriella
...
BMC Medical Genomics. 17 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1186/..
?
2
Sodium Channel Gene Variants in Fetuses with Abnormal Sonog..:
Hadjipanteli, Andrea
;
Theodosiou, Athina
;
Papaevripidou, Ioannis
...
Genes. 15 (2024) 1 - p. 119 , 2024
Link:
https://doi.org/10.3390/..
?
3
CHD2 pathogenic nonsense variant in a three-generation fami..:
Angelopoulou, Eleni
;
Theodosiou, Athina
;
Papaevripidou, Ioannis
...
Heliyon. 9 (2023) 12 - p. e22987 , 2023
Link:
https://doi.org/10.1016/..
?
4
GAA variants associated with reduced enzymatic activity but..:
Malekkou, Anna
;
Theodosiou, Athina
;
Alexandrou, Angelos
...
Molecular Genetics and Metabolism Reports. 36 (2023) - p. 100997 , 2023
Link:
https://doi.org/10.1016/..
?
5
Hereditary multiple exostoses caused by a chromosomal inver..:
Alexandrou, Angelos
;
Salameh, Nicole
;
Papaevripidou, Ioannis
...
Molecular Cytogenetics. 16 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1186/..
?
6
Exploring the Genetic Causality of Discordant Phenotypes in..:
Aristidou, Constantia
;
Theodosiou, Athina
;
Alexandrou, Angelos
...
Genes. 14 (2022) 1 - p. 82 , 2022
Link:
https://doi.org/10.3390/..
?
7
Unravelling the genetic causes of multiple malformation syn..:
Kritioti, Evie
;
Theodosiou, Athina
;
Parpaite, Thibaud
...
PLOS ONE. 16 (2021) 7 - p. e0253562 , 2021
Link:
https://doi.org/10.1371/..
?
8
Novel pericentric inversion inv(9)(p23q22.3) in unrelated i..:
Sismani, Carolina
;
Rapti, Stamatia-Maria
;
Iliopoulou, Pavlina
...
Journal of Human Genetics. 65 (2020) 9 - p. 783-795 , 2020
Link:
https://doi.org/10.1038/..
?
9
An unusual combination of an atypical maternally inherited ..:
Evangelidou, Paola
;
Kousoulidou, Ludmila
;
Salameh, Nicole
...
European Journal of Medical Genetics. 63 (2020) 12 - p. 104084 , 2020
Link:
https://doi.org/10.1016/..
?
10
De novo mosaic MECP2 mutation in a female with Rett syndrom:
Alexandrou, Angelos
;
Papaevripidou, Ioannis
;
Alexandrou, Ioanna Maria
...
Clinical Case Reports. 7 (2019) 2 - p. 366-370 , 2019
Link:
https://doi.org/10.1002/..
?
11
Two unrelated individuals carrying rare mosaic deletions in..:
Kousoulidou, Ludmila
;
Alexandrou, Angelos
;
Papaevripidou, Ioannis
...
American Journal of Medical Genetics Part A. 179 (2018) 1 - p. 134-138 , 2018
Link:
https://doi.org/10.1002/..
?
12
Aniridia due to a novel microdeletion affecting $$\textit{P..:
Syrimis, Andreas
;
Nicolaou, Nayia
;
Alexandrou, Angelos
...
Journal of Genetics. 97 (2018) 2 - p. 555-562 , 2018
Link:
https://doi.org/10.1007/..
?
13
Position effect, cryptic complexity, and direct gene disrup..:
Aristidou, Constantia
;
Theodosiou, Athina
;
Bak, Mads
...
PLOS ONE. 13 (2018) 10 - p. e0205298 , 2018
Link:
https://doi.org/10.1371/..
?
14
Deletion of SNURF/SNRPN U1B and U1B* upstream exons in a ch..:
KOUFARIS, COSTAS
;
ALEXANDROU, ANGELOS
;
PAPAEVRIPIDOU, IOANNIS
...
Journal of Genetics. 95 (2016) 3 - p. 621-624 , 2016
Link:
https://doi.org/10.1007/..
?
15
Identification of a novel 15.5 kb SHOX deletion associated ..:
ALEXANDROU, ANGELOS
;
PAPAEVRIPIDOU, IOANNIS
;
TSANGARAS, KYRIAKOS
...
Journal of Genetics. 95 (2016) 4 - p. 839-845 , 2016
Link:
https://doi.org/10.1007/..
1-15