Skip navigation
Home
Browse
Communities
& Collections
Browse Items by:
Issue Date
Author
Title
Subject
Item Type
Advanced Search
Help
About DSpace
Sign on to:
My DSpace
Receive email
updates
Edit Profile
Saved Searches
Favorites
Repository of UOI "Olympias"
Repository of OAI
Browsing by Author Syrrou, M.
Jump to:
0-9
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
Jump to:
Α
Β
Γ
Δ
Ε
Ζ
Η
Θ
Ι
Κ
Λ
Μ
Ν
Ξ
Ο
Π
Ρ
Σ
Τ
Υ
Φ
Χ
Ψ
Ω
or enter first few letters:
View Option
Sort by:
title
issue date
submit date
In order:
Ascending
Descending
Results/Page
5
10
15
20
25
30
35
40
45
50
55
60
65
70
75
80
85
90
95
100
Authors/Record:
All
1
5
10
15
20
25
30
35
40
45
50
Showing results 25 to 44 of 46
< previous
next >
Title
Author(s)
Issue date
???itemlist.???
Kennedy disease: avoiding misdiagnosis
Paparounas, K.
;
Gotsi, A.
;
Syrrou, M.
;
Akritidis, N.
24-Nov-2015
-
Lack of association of birth size with polymorphisms of two imprinted genes, IGF2R and GRB10
Kukuvitis, A.
;
Georgiou, I.
;
Syrrou, M.
;
Andronikou, S.
;
Dickerman, Z.
;
Islam, A.
;
McCann, J.
;
Polychronakos, C.
24-Nov-2015
-
Martin-Bell syndrome in Greece, with report of another 47,XXY fragile X patient
Mavrou, A.
;
Syrrou, M.
;
Tsenghi, C.
;
Agelakis, M.
;
Youroukos, S.
;
Metaxotou, C.
24-Nov-2015
-
Methylation status of the SNRPN and HUMARA genes in testicular biopsy samples
Dasoula, A.
;
Georgiou, I.
;
Kontogianni, E.
;
Sofikitis, N.
;
Syrrou, M.
24-Nov-2015
-
Molecular cytogenetic characterization and origin of two de novo duplication 9p cases
Tsezou, A.
;
Kitsiou, S.
;
Galla, A.
;
Petersen, M. B.
;
Karadima, G.
;
Syrrou, M.
;
Sahlen, S.
;
Blennow, E.
24-Nov-2015
-
Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: incidence, genetic variation, and stability
Patsalis, P. C.
;
Sismani, C.
;
Hettinger, J. A.
;
Boumba, I.
;
Georgiou, I.
;
Stylianidou, G.
;
Anastasiadou, V.
;
Koukoulli, R.
;
Pagoulatos, G.
;
Syrrou, M.
24-Nov-2015
-
Mosaic trisomy r(14) associated with epilepsy and mental retardation
Tzoufi, M.
;
Kanioglou, C.
;
Dasoula, A.
;
Asproudis, I.
;
Tsatsoulis, A.
;
Sismani, C.
;
Patsalis, P. C.
;
Georgiou, I.
;
Syrrou, M.
24-Nov-2015
-
Mosaicism for duplication 12q (12q13-->12q21.2) accompanied by a pericentric inversion in a dysmorphic female infant
Vermeesch, J. R.
;
Syrrou, M.
;
Salden, I.
;
Dhondt, F.
;
Matthijs, G.
;
Fryns, J. P.
24-Nov-2015
-
Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia
Schlingmann, K. P.
;
Sassen, M. C.
;
Weber, S.
;
Pechmann, U.
;
Kusch, K.
;
Pelken, L.
;
Lotan, D.
;
Syrrou, M.
;
Prebble, J. J.
;
Cole, D. E.
;
Metzger, D. L.
;
Rahman, S.
;
Tajima, T.
;
Shu, S. G.
;
Waldegger, S.
;
Seyberth, H. W.
;
Konrad, M.
24-Nov-2015
-
Oestrogen receptor gene polymorphisms and ovarian stimulation for in-vitro fertilization
Georgiou, I.
;
Konstantelli, M.
;
Syrrou, M.
;
Messinis, I. E.
;
Lolis, D. E.
24-Nov-2015
-
Promoter hypermethylation of the MEG3 (DLK1/MEG3) imprinted gene in multiple myeloma
Benetatos, L.
;
Dasoula, A.
;
Hatzimichael, E.
;
Georgiou, I.
;
Syrrou, M.
;
Bourantas, K. L.
24-Nov-2015
-
Refining the locus of branchio-otic syndrome 2 (BOS2) to a 5.25 Mb locus on chromosome 1q31.3q32.1
Thienpont, B.
;
Dimitriadou, E.
;
Theodoropoulos, K.
;
Breckpot, J.
;
Fryssira, H.
;
Kitsiou-Tzeli, S.
;
Tzoufi, M.
;
Vermeesch, J. R.
;
Syrrou, M.
;
Devriendt, K.
24-Nov-2015
-
Refractory photosensitive epilepsy associated with a complex rearrangement of chromosome 2
Van Esch, H.
;
Syrrou, M.
;
Lagae, L.
24-Nov-2015
-
Retrotransposon RNA expression and evidence for retrotransposition events in human oocytes
Georgiou, I.
;
Noutsopoulos, D.
;
Dimitriadou, E.
;
Markopoulos, G.
;
Apergi, A.
;
Lazaros, L.
;
Vaxevanoglou, T.
;
Pantos, K.
;
Syrrou, M.
;
Tzavaras, T.
24-Nov-2015
-
The role of stress in female reproduction and pregnancy: an update
Vrekoussis, T.
;
Kalantaridou, S. N.
;
Mastorakos, G.
;
Zoumakis, E.
;
Makrigiannakis, A.
;
Syrrou, M.
;
Lavasidis, L. G.
;
Relakis, K.
;
Chrousos, G. P.
24-Nov-2015
-
Seckel syndrome in a family with three affected children and hematological manifestations associated with chromosome instability
Syrrou, M.
;
Georgiou, I.
;
Paschopoulos, M.
;
Lolis, D.
24-Nov-2015
-
Skewed X-chromosome inactivation in Greek women with idiopathic recurrent miscarriage
Dasoula, A.
;
Kalantaridou, S.
;
Sotiriadis, A.
;
Pavlou, M.
;
Georgiou, I.
;
Paraskevaidis, E.
;
Makrigiannakis, A.
;
Syrrou, M.
24-Nov-2015
-
Supernumerary marker chromosomes (SMCs) in Turner syndrome are mostly derived from the Y chromosome
Patsalis, P. C.
;
Hadjimarcou, M. I.
;
Velissariou, V.
;
Kitsiou-Tzeli, S.
;
Zera, C.
;
Syrrou, M.
;
Lyberatou, E.
;
Tsezou, A.
;
Galla, A.
;
Skordis, N.
24-Nov-2015
-
Unusual chromosomal mosaicism in Wolf-Hirschhorn syndrome: del(4)(p16)/der(4)(qter-q31.3::pter-qter)
Syrrou, M.
;
Borghgraef, M.
;
Fryns, J. P.
24-Nov-2015
-
Variation in the number of FMR1 microsatellite repeats in three subgroups of the Hellenic population
Syrrou, M.
;
Patsalis, P. C.
;
Georgiou, I.
;
Alamanos, Y.
;
Pagoulatos, G.
24-Nov-2015
-