Retrotransposon RNA expression and evidence for retrotransposition events in human oocytes
Georgiou, Ioannis, Noutsopoulos, Dimitrios, Dimitriadou, Eftychia, Markopoulos, Georgios, Apergi, Anastasia, Lazaros, Leandros, Vaxevanoglou, Terpsi, Pantos, Kostas, Syrrou, Maria, Tzavaras, Theodore
Published in Human molecular genetics (01.04.2009)
Published in Human molecular genetics (01.04.2009)
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Alpha-thalassemia intellectual disability: variable phenotypic expression among males with a recurrent nonsense mutation - c.109C>T (p.R37X)
Basehore, M.J., Michaelson-Cohen, R., Levy-Lahad, E., Sismani, C., Bird, L.M., Friez, M.J., Walsh, T., Abidi, F., Holloway, L., Skinner, C., McGee, S., Alexandrou, A., Syrrou, M., Patsalis, P.C., Raymond, G., Wang, T., Schwartz, C.E., King, M.-C., Stevenson, R.E.
Published in Clinical genetics (01.05.2015)
Published in Clinical genetics (01.05.2015)
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Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations
Witsch-Baumgartner, M, Schwentner, I, Gruber, M, Benlian, P, Bertranpetit, J, Bieth, E, Chevy, F, Clusellas, N, Estivill, X, Gasparini, G, Giros, M, Kelley, R I, Krajewska-Walasek, M, Menzel, J, Miettinen, T, Ogorelkova, M, Rossi, M, Scala, I, Schinzel, A, Schmidt, K, Schönitzer, D, Seemanova, E, Sperling, K, Syrrou, M, Talmud, P J, Wollnik, B, Krawczak, M, Labuda, D, Utermann, G
Published in Journal of medical genetics (01.04.2008)
Published in Journal of medical genetics (01.04.2008)
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Journal Article
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.
Published in Fetal diagnosis and therapy (01.01.2008)
Published in Fetal diagnosis and therapy (01.01.2008)
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Oestrogen receptor gene polymorphisms and ovarian stimulation for in-vitro fertilization
Georgiou, I, Konstantelli, M, Syrrou, M, Messinis, I E, Lolis, D E
Published in Human reproduction (Oxford) (01.07.1997)
Published in Human reproduction (Oxford) (01.07.1997)
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In-utero stress and mode of conception: impact on regulation of imprinted genes, fetal development and future health
Argyraki, Maria, Damdimopoulou, Pauliina, Chatzimeletiou, Katerina, Grimbizis, Grigoris F, Tarlatzis, Basil C, Syrrou, Maria, Lambropoulos, Alexandros
Published in Human reproduction update (05.11.2019)
Published in Human reproduction update (05.11.2019)
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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.
Published in Journal of Pediatric Endocrinology and Metabolism (01.09.2004)
Published in Journal of Pediatric Endocrinology and Metabolism (01.09.2004)
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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
Published in Journal of medical genetics (01.11.2002)
Published in Journal of medical genetics (01.11.2002)
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Chromomycin A3-staining as an indicator of protamine deficiency and fertilization
Lolis, D, Georgiou, I, Syrrou, M, Zikopoulos, K, Konstantelli, M, Messinis, I
Published in International journal of andrology (01.02.1996)
Published in International journal of andrology (01.02.1996)
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Induction and memory effects in the UV laser ablation of weakly absorbing van der Waals films
Georgiou, S., Koubenakis, A., Kontoleta, P., Syrrou, M.
Published in Chemical physics letters (20.09.1996)
Published in Chemical physics letters (20.09.1996)
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Abeta apolipoprotenaemia as a very rare cause of secondary amenorrhea
Tzouma, Christina, Milionis, H., Hatzidakis, V.E., Syrrou, M., Messaropoulos, P., Oikonomou, M., Koutoulakis, I., Drakakis, P., Kalantaridou, S.
Published in Maturitas (01.06.2017)
Published in Maturitas (01.06.2017)
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Analysis of chromosomal aberrations in breast cancer by comparative genomic hybridization (CGH). Correlation with histoprognostic variables and c-erbB-2 immunoexpression
Malamou-Mitsi, V D, Syrrou, M, Georgiou, I, Pagoulatos, G, Agnantis, N J
Published in Journal of experimental & clinical cancer research (01.09.1999)
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Published in Journal of experimental & clinical cancer research (01.09.1999)
Journal Article
Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6 , a new member of the TRPM gene family
Sassen, Martin, Kratz, Markus, Haddad, Elie, Syrrou, Maria, Konrad, Martin, Weber, Stefanie, Niemann Nejsum, Lene, Klingel, Karin, Nielsen, Søren, Ristoff, Ellinor, Peters, Melanie, Vitzthum, Helga, Dinour, Dganit, Waldegger, Siegfried, Seyberth, Hannsjörg W, Schlingmann, Karl P
Published in Nature genetics (01.06.2002)
Published in Nature genetics (01.06.2002)
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Effect of Percoll gradient and swim-up preparation on the chromomycin A3 staining of normal and abnormal semen samples
Georgiou, I., Syrrou, M., Stefanidis, K., Konstantelli, M., Lolis, D.
Published in Andrologia (01.03.1998)
Published in Andrologia (01.03.1998)
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Journal Article
Conference Proceeding
Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia
SCHLINGMANN, Karl P, SASSEN, Martin C, METZGER, Daniel L, RAHMAN, Shamima, TAJIMA, Toshihiro, SHU, San-Ging, WALDEGGER, Siegfried, SEYBERTH, Hannsjoerg W, KONRAD, Martin, WEBER, Stefanie, PECHMANN, Ulla, KUSCH, Kerstin, PELKEN, Lutz, LOTAN, Daniel, SYRROU, Maria, PREBBLE, Jeffrey J, COLE, David E. C
Published in Journal of the American Society of Nephrology (01.10.2005)
Published in Journal of the American Society of Nephrology (01.10.2005)
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