Massively parallel sequencing reveals the complex structure of an irradiated human chromosome on a mouse background in the Tc1 model of Down syndrome von Gribble, Susan M, Wiseman, Frances K, Clayton, Stephen, Prigmore, Elena, Langley, Elizabeth, Yang, Fengtang, Maguire, Sean, Fu, Beiyuan, Rajan, Diana, Sheppard, Olivia, Scott, Carol, Hauser, Heidi, Stephens, Philip J, Stebbings, Lucy A, Ng, Bee Ling, Fitzgerald, Tomas, Quail, Michael A, Banerjee, Ruby, Rothkamm, Kai, Tybulewicz, Victor L J, Fisher, Elizabeth M C, Carter, Nigel P

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Auditory function in the Tc1 mouse model of down syndrome suggests a limited region of human chromosome 21 involved in otitis media von Kuhn, Stephanie, Ingham, Neil, Pearson, Selina, Gribble, Susan M, Clayton, Stephen, Steel, Karen P, Marcotti, Walter

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Array painting: a protocol for the rapid analysis of aberrant chromosomes using DNA microarrays von Gribble, Susan M, Ng, Bee Ling, Prigmore, Elena, Fitzgerald, Tomas, Carter, Nigel P

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Breakpoint Mapping and Array CGH in Translocations: Comparison of a Phenotypically Normal and an Abnormal Cohort von Baptista, Julia, Mercer, Catherine, Prigmore, Elena, Gribble, Susan M., Carter, Nigel P., Maloney, Viv, Thomas, N. Simon, Jacobs, Patricia A., Crolla, John A.

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UBE2QL1 is Disrupted by a Constitutional Translocation Associated with Renal Tumor Predisposition and is a Novel Candidate Renal Tumor Suppressor Gene von Wake, Naomi C., Ricketts, Christopher J., Morris, Mark R., Prigmore, Elena, Gribble, Susan M., Skytte, Anne-Bine, Brown, Michael, Clarke, Noel, Banks, Rosamonde E., Hodgson, Shirley, Turnell, Andrew S., Maher, Eamonn R., Woodward, Emma R.

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Heterogeneous Duplications in Patients with Pelizaeus-Merzbacher Disease Suggest a Mechanism of Coupled Homologous and Nonhomologous Recombination von Woodward, Karen J., Cundall, Maria, Sperle, Karen, Sistermans, Erik A., Ross, Mark, Howell, Gareth, Gribble, Susan M., Burford, Deborah C., Carter, Nigel P., Hobson, Donald L., Garbern, James Y., Kamholz, John, Heng, Henry, Hodes, M.E., Malcolm, Sue, Hobson, Grace M.

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Finishing the finished human chromosome 22 sequence von Cole, Charlotte G, McCann, Owen T, Collins, John E, Oliver, Karen, Willey, David, Gribble, Susan M, Yang, Fengtang, McLaren, Karen, Rogers, Jane, Ning, Zemin, Beare, David M, Dunham, Ian

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Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridization von Freitas, Érika L., Gribble, Susan M., Simioni, Milena, Vieira, Társis P., Silva‐Grecco, Roseane L., Balarin, Marly A. S., Prigmore, Elena, Krepischi‐Santos, Ana C., Rosenberg, Carla, Szuhai, Karoly, van Haeringen, Arie, Carter, Nigel P., Gil‐da‐Silva‐Lopes, Vera Lúcia

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A familial case with interstitial 2q36 deletion: Variable phenotypic expression in full and mosaic state von Freitas, Érika L, Gribble, Susan M, Simioni, Milena, Vieira, Társis P, Prigmore, Elena, Krepischi, Ana C, Rosenberg, Carla, Pearson, Peter L, Melo, Débora G, Gil-da-Silva-Lopes, Vera Lúcia

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Molecular cytogenetic analyses of breakpoints in apparently balanced reciprocal translocations carried by phenotypically normal individuals von Baptista, Julia, Prigmore, Elena, Gribble, Susan M, Jacobs, Patricia A, Carter, Nigel P, Crolla, John A

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Micro-array analyses decipher exceptional complex familial chromosomal rearrangement von FAUTH, Christine, GRIBBLE, Susan M, CARTER, Nigel P, SPEICHER, Michael R, PORTER, Keith M, CODINA-PASCUAL, Montserrat, BEE LING NG, KRAUS, Jiirgen, UHRIG, Sabine, LEIFHEIT, Jürgen, HAAF, Thomas, FIEGLER, Heike

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SmartCapture and the frontiers of FISH technology: report of the Digital Scientific UK SmartCapture User's Meeting, Peterhouse College Cambridge, UK, 2nd September 2005 von Reid, Alistair G, Gribble, Susan M

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Genomic imbalances in CML blast crisis: 8q24.12-q24.13 Segment identified as a common region of over-representation von Gribble, Susan M., Reid, Alistair G., Roberts, Ian, Grace, Colin, Green, Anthony R., Nacheva, Elizabeth P.

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Cloning of a new familial t(3;8) translocation associated with conventional renal cell carcinoma reveals a 5 kb microdeletion and no gene involved in the rearrangement von Rodríguez-Perales, Sandra, Meléndez, Bárbara, Gribble, Susan M., Valle, Laura, Carter, Nigel P., Santamaría, Iñigo, Conde, Lucia, Urioste, Miguel, Benítez, Javier, Cigudosa, Juan C.

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Variant Philadelphia translocations in chronic myeloid leukaemia can mimic typical blast crisis chromosome abnormalities or classic t(9;22): a report of two cases von Reid, Alistair, Gribble, Susan M., Huntly, Brian J. P., Andrews, Kathryn M., Campbell, Lynda, Grace, Colin D., Wood, Marion E., Green, Anthony R., Nacheva, Ellie P.

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UBE 2 QL 1 is Disrupted by a Constitutional Translocation Associated with Renal Tumor Predisposition and is a Novel Candidate Renal Tumor Suppressor Gene von Wake, Naomi C., Ricketts, Christopher J., Morris, Mark R., Prigmore, Elena, Gribble, Susan M., Skytte, Anne‐Bine, Brown, Michael, Clarke, Noel, Banks, Rosamonde E., Hodgson, Shirley, Turnell, Andrew S., Maher, Eamonn R., Woodward, Emma R.

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Massively Parallel Sequencing Reveals the Complex Structure of an Irradiated Human Chromosome on a Mouse Background in the Tc1 Model of Down Syndrome. e60482 von Gribble, Susan M, Wiseman, Frances K, Clayton, Stephen, Prigmore, Elena, Langley, Elizabeth, Yang, Fengtang, Maguire, Sean, Fu, Beiyuan, Rajan, Diana, Sheppard, Olivia

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Comparative Analysis of G-Banding, Chromosome Painting, Locus-Specific Fluorescence In Situ Hybridization, and Comparative Genomic Hybridization in Chronic Myeloid Leukemia Blast C... von Gribble, Susan M, Sinclair, Paul B, Grace, Colin, Green, Anthony R, Nacheva, Elizabeth P

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Cytogenetics of the Chronic Myeloid Leukemia-Derived Cell Line K562: Karyotype Clarification by Multicolor Fluorescence In Situ Hybridization, Comparative Genomic Hybridization, an... von Gribble, Susan M, Roberts, Ian, Grace, Colin, Andrews, Kathryn M, Green, Anthony R, Nacheva, Elizabeth P

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Cloning of a new familial t(3; 8) translocation associated with conventional renal cell carcinoma reveals a 5kb microdeletion and no gene involved in the rearrangement von Rodriguez-Perales, Sandra, Melendez, Barbara, Gribble, Susan M, Valle, Laura, Carter, Nigel P, Santamaria, Inigo, Conde, Lucia, Urioste, Miguel, Benitez, Javier, Cigudosa, Juan C

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