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Results:
1-11
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Results: 11
Authors:
Syrrou, M
Borghgraef, M
Fryns, JP
Citation: M. Syrrou et al., Unusual chromosomal mosaicism in Wolf-Hirschhorn syndrome: del(4)(p16)/der(4)(qter-q31.3 :: pter-qter), AM J MED G, 104(3), 2001, pp. 199-203
Authors:
Syrrou, M
Fryns, JP
Citation: M. Syrrou et Jp. Fryns, Interstitial deletion of chromosome 11 (q22.3-q23.2) in a boy with mild developmental delay, J MED GENET, 38(9), 2001, pp. 621-624
Authors:
Frints, SGM
Fryns, JP
Lagae, L
Syrrou, M
Marynen, P
Devriendt, K
Citation: Sgm. Frints et al., Xp22.3;Yq11.2 chromosome translocation and its clinical manifestations, ANN GENET, 44(2), 2001, pp. 71-76
Authors:
Van Buggenhout, GJCM
van Ravenswaaij-Arts, C
Mieloo, H
Syrrou, M
Hamel, B
Brunner, H
Fryns, JP
Citation: Gjcm. Van Buggenhout et al., Dysmorphology and mental retardation: molecular cytogenetic studies in dysmorphic mentally retarded patients, ANN GENET, 44(2), 2001, pp. 89-92
Authors:
Rosser,"Efgrafov, O
Syrrou, M
Meitinger, TA
Rubinsztein, DC
Stefanescu, G
Tolun, A
Citation: O. Rosser,"efgrafov et al., Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language (vol 67, pg 1526, 2000), AM J HU GEN, 68(4), 2001, pp. 1075-1075
Authors:
Tsezou, A
Kitsiou, S
Galla, A
Petersen, MB
Karadima, G
Syrrou, M
Sahlen, S
Blennow, E
Citation: A. Tsezou et al., Molecular cytogenetic characterization and origin of two de novo duplication 9p cases, AM J MED G, 91(2), 2000, pp. 102-106
Authors:
Malamou-Mitsi, VD
Syrrou, M
Georgiou, I
Pagoulatos, G
Agnantis, NJ
Citation: Vd. Malamou-mitsi et al., Analysis of chromosomal aberrations in breast cancer by comparative genomic hybridization (CGH). Correlation with histoprognostic variables and c-erbB-2 immunoexpression, J EXP CL C, 18(3), 1999, pp. 357-361
Authors:
Patsalis, PC
Sismani, C
Hettinger, JA
Boumba, I
Georgiou, I
Stylianidou, G
Anastasiadou, V
Koukoulli, R
Pagoulatos, G
Syrrou, M
Citation: Pc. Patsalis et al., Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: Incidence, genetic variation, and stability, AM J MED G, 84(3), 1999, pp. 184-190
Authors:
Syrrou, M
Georgiou, I
Patsalis, PC
Bouba, I
Adonakis, G
Papoulatos, GN
Citation: M. Syrrou et al., Fragile X premutations and (TA)n estrogen receptor polymorphism in women with ovarian dysfunction, AM J MED G, 84(3), 1999, pp. 306-308
Authors:
Allingham-Hawkins, SJ
Babul-Hirji, R
Chitayat, D
Holden, JJA
Yang, KT
Lee, C
Hudson, R
Gorwill, H
Nolin, SL
Glicksman, A
Jenkins, EC
Brown, WT
Howard-Peebles, PN
Becchi, C
Cummings, E
Fallon, L
Seitz, S
Black, SH
Vianna-Morgante, AM
Costa, SS
Otto, PA
Mingroni-Netto, RC
Murray, A
Webb, J
MacSwinney, F
Dennis, N
Jacobs, PA
Syrrou, M
Georgiou, I
Patsalis, PC
Uzielli, MLG
Guarducci, S
Lapi, E
Cecconi, A
Ricci, U
Citation: Sj. Allingham-hawkins et al., Fragile X premutation is a significant risk factor for premature ovarian failure: The international collaborative POF in fragile X study - Preliminary data, AM J MED G, 83(4), 1999, pp. 322-325
Authors:
Georgiou, I
Syrrou, M
Bouba, I
Dalkalitsis, N
Paschopoulos, M
Navrozoglou, I
Lolis, D
Citation: I. Georgiou et al., Association of estrogen receptor gene polymorphisms with endometriosis, FERT STERIL, 72(1), 1999, pp. 164-166
Risultati:
1-11
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