Investigation of the glucocorticoid receptor co-chaperone FKBP5 in individuals with first-episode psychosis von Theodoridou, D., Vlaikou, A. M., Karampas, A., Georgiou, G., Filiou, M.D., Syrrou, M., Petrikis, P.

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Retrotransposon RNA expression and evidence for retrotransposition events in human oocytes von Georgiou, Ioannis, Noutsopoulos, Dimitrios, Dimitriadou, Eftychia, Markopoulos, Georgios, Apergi, Anastasia, Lazaros, Leandros, Vaxevanoglou, Terpsi, Pantos, Kostas, Syrrou, Maria, Tzavaras, Theodore

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In-utero stress and mode of conception: impact on regulation of imprinted genes, fetal development and future health von Argyraki, Maria, Damdimopoulou, Pauliina, Chatzimeletiou, Katerina, Grimbizis, Grigoris F, Tarlatzis, Basil C, Syrrou, Maria, Lambropoulos, Alexandros

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Alpha-thalassemia intellectual disability: variable phenotypic expression among males with a recurrent nonsense mutation - c.109C>T (p.R37X) von 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.

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Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations von 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

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Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6 , a new member of the TRPM gene family von 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

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Skewed X-Chromosome Inactivation in Greek Women with Idiopathic Recurrent Miscarriage von Dasoula, A., Kalantaridou, S., Sotiriadis, A., Pavlou, M., Georgiou, I., Paraskevaidis, E., Makrigiannakis, A., Syrrou, M.

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Abeta apolipoprotenaemia as a very rare cause of secondary amenorrhea von Tzouma, Christina, Milionis, H., Hatzidakis, V.E., Syrrou, M., Messaropoulos, P., Oikonomou, M., Koutoulakis, I., Drakakis, P., Kalantaridou, S.

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Refractory Photosensitive Epilepsy Associated with a Complex Rearrangement of Chromosome 2 von Van Esch, H., Syrrou, M., Lagae, L.

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Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia von 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

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Oestrogen receptor gene polymorphisms and ovarian stimulation for in-vitro fertilization von Georgiou, I, Konstantelli, M, Syrrou, M, Messinis, I E, Lolis, D E

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Interstitial deletion of chromosome 11 (q22.3-q23.2) in a boy with mild developmental delay von Syrrou, M, Fryns, J-P

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Chromomycin A3-staining as an indicator of protamine deficiency and fertilization von LOLIS, D., GEORGIOU, I., SYRROU, M., ZIKOPOULOS, K., KONSTANTELLI, M., MESSINIS, I.

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Mosaicism for duplication 12q (12q13→12q21.2) accompanied by a pericentric inversion in a dysmorphic female infant von Vermeesch, J R, Syrrou, M, Salden, I, Dhondt, F, Matthijs, G, Fryns, J-P

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Alpha‐thalassemia intellectual disability: variable phenotypic expression among males with a recurrent nonsense mutation – c. 109C >T (p. R37X ) von 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.

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Association of estrogen receptor gene polymorphisms with endometriosis von Georgiou, Ioannis, Syrrou, Maria, Bouba, Ioanna, Dalkalitsis, Nikolaos, Paschopoulos, Minas, Navrozoglou, Iordanis, Lolis, Dimitrios

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Induction and memory effects in the UV laser ablation of weakly absorbing van der Waals films von Georgiou, S., Koubenakis, A., Kontoleta, P., Syrrou, M.

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Effect of Percoll gradient and swim-up preparation on the chromomycin A3 staining of normal and abnormal semen samples von Georgiou, I., Syrrou, M., Stefanidis, K., Konstantelli, M., Lolis, D.

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Infertility and Multiple Urogenital Abnormalities in a Male with Mosaic 46,XY/45,XO/47,XXY Karyotype and Mixed Phenotype von Filiadis, Ioannis F., Syrrou, Maria B., Bai, Maria C., Georgiou, Ioannis A., Pagoulatos, Gerasimos N., Giannakopoulos, Xenophon

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Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations von 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

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