High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH
BRUDER, Carl E. G, HIRVELÄ, Carina, ZUCMAN-ROSSI, Jessica, HERGERSBERG, Martin, BOLTSHAUSER, Eugene, PAPI, Laura, ROULEAU, Guy A, POPTODOROV, George, JORDANOVA, Albena, RASK-ANDERSEN, Helge, KLUWE, Lan, MAUTNER, Victor, TAPIA-PAEZ, Isabel, SAINIO, Markku, HUNG, Gene, MATHIESEN, Tiit, MÖLLER, Claes, PULST, Stefan M, HARDER, Henrik, HEIBERG, Arvid, HONDA, Mariko, NIIMURA, Michihito, SAHLEN, Sigrid, FRANSSON, Ingegerd, BLENNOW, Elisabeth, ALBERTSON, Donna G, PINKEL, Daniel, DUMANSKI, Jan P, SEGRAVES, Richard, HAMILTON, Greg, XIAO XIAO ZHANG, EVANS, D. Gareth, WALLACE, Andrew J, BASER, Michael E
Published in Human molecular genetics (01.02.2001)
Published in Human molecular genetics (01.02.2001)
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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 leukaemia: detailed analysis of 70 cases
NORDGREN, Ann, HEYMAN, Mats, SAHLEN, Sigrid, SCHOUMANS, Jacqueline, SÖDERHÄLL, Stefan, NORDENSKJÖLD, Magnus, BLENNOW, Elisabeth
Published in European journal of haematology (2002)
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Detailed molecular and clinical characterization of three patients with 21q deletions
Lindstrand, A, Malmgren, H, Sahlén, S, Schoumans, J, Nordgren, A, Ergander, U, Holm, E, Anderlid, BM, Blennow, E
Published in Clinical genetics (01.02.2010)
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Comparative genomic hybridization and karyotyping of human embryonic stem cells reveals the occurrence of an isodicentric X chromosome after long‐term cultivation
Inzunza, J., Sahlén, S., Holmberg, K., Strömberg, A.‐M., Teerijoki, H., Blennow, E., Hovatta, O., Malmgren, H.
Published in Molecular human reproduction (01.06.2004)
Published in Molecular human reproduction (01.06.2004)
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Semantic Processing in Deaf and Hard-of-Hearing Children: Large N400 Mismatch Effects in Brain Responses, Despite Poor Semantic Ability
Kallioinen, Petter, Olofsson, Jonas, Nakeva von Mentzer, Cecilia, Lindgren, Magnus, Ors, Marianne, Sahlén, Birgitta S, Lyxell, Björn, Engström, Elisabet, Uhlén, Inger
Published in Frontiers in psychology (2016)
Published in Frontiers in psychology (2016)
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Molecular cytogenetic characterization of a constitutional, highly complex intrachromosomal rearrangement of chromosome 1, with 14 breakpoints and a 0.5 Mb submicroscopic deletion
Lindstrand, A., Malmgren, H., Sahlén, S., Xin, H., Schoumans, J., Blennow, E.
Published in American journal of medical genetics. Part A (15.12.2008)
Published in American journal of medical genetics. Part A (15.12.2008)
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Fine mapping of the constitutional translocation t(11;22)(q23;q11)
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
Published in Human genetics (01.05.2000)
Published in Human genetics (01.05.2000)
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Concurrent microdeletion and duplication of 22q11.2
Blennow, E, Lagerstedt, K, Malmgren, H, Sahlén, S, Schoumans, J, Anderlid, BM
Published in Clinical genetics (01.07.2008)
Published in Clinical genetics (01.07.2008)
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P2816Left atrial volume is an independent predictor of outcome in a large asian cohort with acute heart failure
Go, Y Y, Chia, S Y, Ewe, S H, Sahlen, S A, Sim, D, Jaufeerally, F R, Ding, Z P, Lim, T K
Published in European heart journal (01.08.2018)
Published in European heart journal (01.08.2018)
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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
Teh, Bin T., Blennow, Elizabeth, Giraud S, Sophie, Sahlén, Sigrid, Hii, Su I., Brookwell, Ross, Brauch, Hiltrud, Nordenskjöld, Magnus, Larsson, Catharina, Nicol, David
Published in Genes chromosomes & cancer (01.03.1998)
Published in Genes chromosomes & cancer (01.03.1998)
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Single cell CGH analysis reveals a high degree of mosaicism in human embryos from patients with balanced structural chromosome aberrations
Malmgren, H., Sahlén, S., Inzunza, J., Aho, M., Rosenlund, B., Fridström, M., Hovatta, O., Ährlund-Richter, L., Nordenskjöld, M., Blennow, E.
Published in Molecular human reproduction (01.05.2002)
Published in Molecular human reproduction (01.05.2002)
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Cloning, Expression Pattern, and Chromosomal Assignment to 16q23 of the Human γ-Adaptin Gene (ADTG)
Peyrard, Myriam, Parveneh, Shahram, Lagercrantz, Svetlana, Ekman, Michelle, Fransson, Ingegerd, Sahlén, Sigrid, Dumanski, Jan P.
Published in Genomics (San Diego, Calif.) (01.06.1998)
Published in Genomics (San Diego, Calif.) (01.06.1998)
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Subtelomeric rearrangements detected in patients with idiopathic mental retardation
Anderlid, Britt-Marie, Schoumans, Jacqueline, Annerén, Göran, Sahlén, Sigrid, Kyllerman, Mårten, Vujic, Mihailo, Hagberg, Bengt, Blennow, Elisabeth, Nordenskjöld, Magnus
Published in American journal of medical genetics (01.02.2002)
Published in American journal of medical genetics (01.02.2002)
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Molecular cytogenetic characterization of an insertional translocation, ins(6;7)(p25;q33q34): Deletion/duplication of 7q33-34 and clinical correlations
Malmgren, H., Malm, G., Sahlén, S., Karlsson, M., Blennow, Elisabeth
Published in American journal of medical genetics. Part A (15.11.2005)
Published in American journal of medical genetics. Part A (15.11.2005)
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Interphase fluorescent in situ hybridization deletion analysis of the 9p21 region and prognosis in childhood acute lymphoblastic leukaemia (ALL): results from a prospective analysis of 519 Nordic patients treated according to the NOPHO‐ALL 2000 protocol
Kuchinskaya, Ekaterina, Heyman, Mats, Nordgren, Ann, Söderhäll, Stefan, Forestier, Erik, Wehner, Peder, Vettenranta, Kim, Jonsson, Olafur, Wesenberg, Finn, Sahlén, Sigrid, Nordenskjöld, Magnus, Blennow, Elisabeth
Published in British journal of haematology (01.03.2011)
Published in British journal of haematology (01.03.2011)
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Distal 3p deletion syndrome: Detailed molecular cytogenetic and clinical characterization of three small distal deletions and review
Malmgren, Helena, Sahlén, Sigrid, Wide, Katarina, Lundvall, Mikael, Blennow, Elisabeth
Published in American journal of medical genetics. Part A (15.09.2007)
Published in American journal of medical genetics. Part A (15.09.2007)
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In vivo differentiated human embryonic stem cells can acquire chromosomal aberrations more frequently than in vitro during the same period
Zucchelli, Marco, Ström, Susanne, Holm, Frida, Malmgren, Helena, Sahlén, Sigrid, Religa, Piotr, Hovatta, Outi, Kere, Juha, Inzunza, José
Published in Stem cells and development (10.12.2012)
Published in Stem cells and development (10.12.2012)
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