Tiling resolution array comparative genomic hybridization, expression and methylation analyses of dup(1q) in Burkitt lymphomas and pediatric high hyperdiploid acute lymphoblastic leukemias reveal clustered near-centromeric breakpoints and overexpression of genes in 1q22-32.3 von Davidsson, Josef, Andersson, Anna, Paulsson, Kajsa, Heidenblad, Markus, Isaksson, Margareth, Borg, Åke, Heldrup, Jesper, Behrendtz, Mikael, Panagopoulos, Ioannis, Fioretos, Thoas, Johansson, Bertil

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Is it possible to implement community care based on mental health in Japan? A comparison between decade ago and present on Duration of Untreated Psychosis (DUP) von Suzuki, Kouta, Niimura, Hidehito, Yamazawa, Ryoko, Nemoto, Takahiro, Murakami, Masaaki, Mimura, Masaru, Mizuno, Masafumi

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dup(10q) lacking α-satellite DNA in bone marrow cells of a patient with acute myeloid leukemia von Abeliovich, Dvorah, Yehuda, Orly, Ben-Neriah, Susana, Kapelushnik, Yosef, Ben-Yehuda, Dina

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The Spoofing Detection of Dynamic Underwater Positioning Systems (DUPS) Based on Vehicles Retrofitted with Acoustic Speakers von Lemieszewski, Łukasz, Radomska-Zalas, Aleksandra, Perec, Andrzej, Dobryakova, Larisa, Ochin, Evgeny

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Isolation and molecular analysis of inv dup(15) and construction of a physical map of a common breakpoint in order to elucidate their mechanism of formation von Wandstrat, A E, Schwartz, S

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Mutation, methylation, and gene expression profiles in dup(1q)-positive pediatric B-cell precursor acute lymphoblastic leukemia von Gunnarsson, Rebeqa, Dilorenzo, Sebastian, Lundin-Ström, Kristina B, Olsson, Linda, Biloglav, Andrea, Lilljebjörn, Henrik, Rissler, Marianne, Wahlberg, Per, Lundmark, Anders, Castor, Anders, Behrendtz, Mikael, Fioretos, Thoas, Paulsson, Kajsa, Isaksson, Anders, Johansson, Bertil

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Pure interstitial dup(6)(q22.31q22.31) - a case report von Sheth, Frenny, Trivedi, Sunil, Andrieux, Joris, Blouin, Jean-Louis, Sheth, Jayesh

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Detailed analysis of 15q11-q14 sequence corrects errors and gaps in the public access sequence to fully reveal large segmental duplications at breakpoints for Prader-Willi, Angelman, and inv dup(15) syndromes von Makoff, Andrew J, Flomen, Rachel H

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Masked inv dup(22)(q11.23), tetrasomy 8 and trisomy 19 in a blast crisis-chronic myeloid leukemia after interrupted Imatinib-treatment von Wafa, Abdulsamad, Almedani, Suher, Liehr, Thomas, Al-Achkar, Walid

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Neocentromere marker chromosome of distal 3q mimicking dup(3q) syndrome phenotype von Izumi, Kosuke, Yamashita, Yukio, Aramaki, Michihiko, Kosaki, Rika, Hosokai, Noboru, Takahashi, Takao, Kosaki, Kenjiro

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De novo unbalanced translocations in Prader-Willi and Angelman syndrome might be the reciprocal product of inv dup(15)s von Rossi, Elena, Giorda, Roberto, Bonaglia, Maria Clara, Candia, Stefania Di, Grechi, Elena, Franzese, Adriana, Soli, Fiorenza, Rivieri, Francesca, Patricelli, Maria Grazia, Saccilotto, Donatella, Bonfante, Aldo, Giglio, Sabrina, Beri, Silvana, Rocchi, Mariano, Zuffardi, Orsetta

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An analphoid marker chromosome inv dup(15)(q26.1qter), detected during prenatal diagnosis and characterized via chromosome microdissection von Mahjoubi, F., Peters, G.B., Malafiej, P., Shalhoub, C., Turner, A., Daniel, A., Hill, R.J.

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Molecular cytogenetic characterization of the first reported case of inv dup del 20p compatible with a U‐type exchange model von Leclercq, Sandrine, Maincent, Kim, Baverel, Françoise, Tessier, Dominique Le, Letourneur, Franck, Lebbar, Aziza, Dupont, Jean‐Michel

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De Novo Unbalanced Translocations in Prader-Willi and Angelman Syndrome Might Be the Reciprocal Product of inv dup von Rossi, Elena, Giorda, Roberto, Bonaglia, Maria Clara, Candia, Stefania Di, Grechi, Elena, Franzese, Adriana, Soli, Fiorenza, Rivieri, Francesca, Patricelli, Maria Grazia, Saccilotto, Donatella, Bonfante, Aldo, Giglio, Sabrina, Beri, Silvana, Rocchi, Mariano, Zuffardi, Orsetta

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Discordant Semilobar Holoprosencephaly in Monozygotic Twins with de novo inv dup(15) Marker Chromosome and de novo Mutation on SHH Gene von Peng, Hsiu-Huei, Kuo, Pao-Lin, Chao, An-Shine, Wang, Tzu-Hao, Chang, Yao-Lung, Soong, Yung-Kuei, Chang, Shuenn-Dyh

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Simultaneous formation of inv dup(15) and dup(15q) in a girl with developmental delay: origin of the abnormal chromosomes von Abeliovich, D, Dagan, J, Werner, M, Lerer, I, Shapira, Y, Meiner, V

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Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31 --> qter) detected in an autistic boy von Carreira, Isabel M, Melo, Joana B, Rodrigues, Carlos, Backx, Liesbeth, Vermeesch, Joris, Weise, Anja, Kosyakova, Nadezda, Oliveira, Guiomar, Matoso, Eunice

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47,X,idic(Y),inv dup(Y): A Non-Mosaic Case of a Phenotypically Normal Boy with Two Different Y Isochromosomes and Neocentromere Formation von Pasantes, J.J., Wimmer, R., Knebel, S., Münch, C., Kelbova, C., Junge, A., Kieback, P., Küpferling, P., Schempp, W.

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Two girls with a de novo Xq rearrangement of paternal origin: t(X;9)(q24;q12) or rea(X)dup q von Vásquez-Velásquez, Ana I, Rivera, Horacio, Castro, Ana G, Jaloma-Cruz, Ana R, Juárez, Clara I, Lara-Navarro, Irving J, Córdova-Fletes, Carlos, Mendoza- Pérez, Paul, García-Ortiz, José E

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Healthy 12-year-old boy with mosaic inv dup(15)(q13) von Loitzsch, Anne, Bartsch, Oliver

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