Interphase fluorescent in situ hybridization deletion analysis of the 9p21 region and prognosis in childhood acute lymphoblastic leukaemia (ALL): results from a prospective analysi... von Kuchinskaya, Ekaterina, Heyman, Mats, Nordgren, Ann, Söderhäll, Stefan, Forestier, Erik, Wehner, Peder, Vettenranta, Kim, Jonsson, Olafur, Wesenberg, Finn, Sahlén, Sigrid, Nordenskjöld, Magnus, Blennow, Elisabeth

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Distal 3p deletion syndrome: Detailed molecular cytogenetic and clinical characterization of three small distal deletions and review von Malmgren, Helena, Sahlén, Sigrid, Wide, Katarina, Lundvall, Mikael, Blennow, Elisabeth

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Jumping translocation in a phenotypically normal male: A study of mosaicism in spermatozoa, lymphocytes, and fibroblasts von Iwarsson, Erik, Sahlén, Sigrid, Nordgren, Ann

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In Vivo Differentiated Human Embryonic Stem Cells Can Acquire Chromosomal Aberrations More Frequently Than In Vitro During the Same Period von Zucchelli, Marco, Ström, Susanne, Holm, Frida, Malmgren, Helena, Sahlén, Sigrid, Religa, Piotr, Hovatta, Outi, Kere, Juha, Inzunza, José

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On the interaction of speakers' voice quality, ambient noise and task complexity with children's listening comprehension and cognition von Lyberg-Åhlander, Viveka, Brännström, K J, Sahlén, Birgitta S

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Spectral karyotyping and interphase FISH reveal abnormalities not detected by conventional G-banding: Implications for treatment stratification of childhood acute lymphoblastic leu... von NORDGREN, Ann, HEYMAN, Mats, SAHLEN, Sigrid, SCHOUMANS, Jacqueline, SÖDERHÄLL, Stefan, NORDENSKJÖLD, Magnus, BLENNOW, Elisabeth

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Semantic Processing in Deaf and Hard-of-Hearing Children: Large N400 Mismatch Effects in Brain Responses, Despite Poor Semantic Ability von Kallioinen, Petter, Olofsson, Jonas, Nakeva von Mentzer, Cecilia, Lindgren, Magnus, Ors, Marianne, Sahlén, Birgitta S, Lyxell, Björn, Engström, Elisabet, Uhlén, Inger

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Subtelomeric rearrangements detected in patients with idiopathic mental retardation von Anderlid, Britt-Marie, Schoumans, Jacqueline, Annerén, Göran, Sahlén, Sigrid, Kyllerman, Mårten, Vujic, Mihailo, Hagberg, Bengt, Blennow, Elisabeth, Nordenskjöld, Magnus

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Children Listen: Psychological and Linguistic Aspects of Listening Difficulties During Development

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P10: High resolution fine mapping of an extremely complex intrachromosomal rearrangement of chromosome 1 involving 13 breakpoints von Sahlén, Sigrid, Malmgren, Helena, Lindstrand, Anna, Schoumans, Jacqueline, Blennow, Elisabeth

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Rescue from the effects of trisomy 13q32→qter owing to skewed X inactivation in a der(X)t(X;13)(p21;q32) carrier von BLENNOW, ELISABETH, SAHLÉN, SIGRID

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Spectral karyotyping and interphase FISH reveal abnormalities not detected by conventional G-banding von Nordgren, Ann, Heyman, Mats, Sahlén, Sigrid, Schoumans, Jacqueline, Söderhäll, Stefan, Nordenskjöld, Magnus, Blennow, Elisabeth

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Fine mapping of the constitutional translocation t(11;22)(q23;q11) von TAPIA-PAEZ, I, O'BRIEN, K. P, BLENNOW, E, DUMANSKI, J. P, KOST-ALIMOVA, M, SAHLEN, S, KEDRA, D, BRUDER, C. E. G, ANDERSSON, B, ROE, B. A, PING HU, IMREH, S

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Bilateral multiple renal oncocytomas and cysts associated with a constitutional translocation (8;9)(q24.1;q34.3) and a rare constitutional VHL missense substitution von Teh, Bin T., Blennow, Elizabeth, Giraud S, Sophie, Sahlén, Sigrid, Hii, Su I., Brookwell, Ross, Brauch, Hiltrud, Nordenskjöld, Magnus, Larsson, Catharina, Nicol, David

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Cloning, Expression Pattern, and Chromosomal Assignment to 16q23 of the Human γ-Adaptin Gene (ADTG) von Peyrard, Myriam, Parveneh, Shahram, Lagercrantz, Svetlana, Ekman, Michelle, Fransson, Ingegerd, Sahlén, Sigrid, Dumanski, Jan P.

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High resolution deletion analysis of conctitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH von Bruder, Carl E. G., Hirvelä, Carina, Tapia-Paez, Isabel, Fransson, Ingegerd, Segraves, Richard, Hamilton, Greg, Zhang, Xiao Xiao, Evans, D. Gareth, Wallace, Andrew J., Baser, Michael E., Zucman-Rossi, Jessica, Hergersberg, Martin, Boltshauser, Eugene, Papi, Laura, Rouleau, Guy A., Poptodorov, George, Jordanova, Albena, Rask-Andersen, Helge, Kluwe, Lan, Mautner, Victor, Sainio, Markku, Hung, Gene, Mathiesen, Tiit, Möller, Claes, Pulst, Stefan M., Harder, Henrik, Heiberg, Arvid, Honda, Mariko, Niimura, Michihito, Sahlén, Sigrid, Blennow, Elisabeth, Albertson, Donna G., Pinkel, David, Dumanski, Jan P.

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The human RAD51/RecA homologue gene is not a candidate gene for Bloom's syndrome von Hellgren, D, Sahlén, S, Ljungqvist, S, Kenne, K

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Detailed characterization of 12 supernumerary ring chromosomes using micro-FISH and search for uniparental disomy von Anderlid, Britt-Marie, Sahlén, Sigrid, Schoumans, Jacqueline, Holmberg, Eva, Åhsgren, Ingegerd, Mortier, Geert, Speleman, Frank, Blennow, Elisabeth

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Unequal SCE is a rare event in homologous recombination between duplicated neo gene fragments in CHO cells von Hellgren, Dennis, Sahlén, Sigrid, Lambert, Bo

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The fragile X mutation does not have any major effect on the expression of the hypoxanthine phosphoribosyltransferase (HPRT) locus in human fibroblasts von STEEN, A.-M, MARCUS, S, SAHLEN, S, NIELSEN, K. B, LAMBERT, B

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