Prenatal detection of Down's syndrome by rapid aneuploidy testing for chromosomes 13, 18, and 21 by FISH or PCR without a full karyotype: a cytogenetic risk assessment von Caine, Allan, Maltby, A Edna, Parkin, C Anthony, Waters, Jonathan J, Crolla, John A

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Prenatal detection of Down's syndrome by rapid aneuploidy testing for chromosomes 13, 18, and 21 by FISH or PCR without a full karyotype : a cytogenetic risk assessment. Commentary von CAINE, Allan, MALTBY, A Edna, PARKIN, C. Anthony, WATERS, Jonathan J, CROLLO, John A, LEUNG, W. C, LAO, T. T

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Mortality in Women with Turner Syndrome in Great Britain: A National Cohort Study von Schoemaker, Minouk J., Swerdlow, Anthony J., Higgins, Craig D., Wright, Alan F., Jacobs, Patricia A.

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Mortality risks in patients with constitutional autosomal chromosome deletions in Britain: a cohort study von Swerdlow, Anthony J., Schoemaker, Minouk J., Higgins, Craig D., Wright, Alan F., Jacobs, Patricia A.

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Recurrent gain of chromosomes 17q and 12 in cultured human embryonic stem cells von Draper, Jonathan S, Smith, Kath, Gokhale, Paul, Moore, Harry D, Maltby, Edna, Johnson, Julie, Meisner, Lorraine, Zwaka, Thomas P, Thomson, James A, Andrews, Peter W

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Adaptation to culture of human embryonic stem cells and oncogenesis in vivo von Baker, Duncan E C, Harrison, Neil J, Maltby, Edna, Smith, Kath, Moore, Harry D, Shaw, Pamela J, Heath, Paul R, Holden, Hazel, Andrews, Peter W

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High-resolution DNA analysis of human embryonic stem cell lines reveals culture-induced copy number changes and loss of heterozygosity von Närvä, Elisa, Autio, Reija, Rahkonen, Nelly, Kong, Lingjia, Harrison, Neil, Kitsberg, Danny, Borghese, Lodovica, Itskovitz-Eldor, Joseph, Rasool, Omid, Dvorak, Petr, Hovatta, Outi, Otonkoski, Timo, Tuuri, Timo, Cui, Wei, Brüstle, Oliver, Baker, Duncan, Maltby, Edna, Moore, Harry D, Benvenisty, Nissim, Andrews, Peter W, Yli-Harja, Olli, Lahesmaa, Riitta

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Cellular differentiation hierarchies in normal and culture-adapted human embryonic stem cells von Enver, Tariq, Soneji, Shamit, Joshi, Chirag, Brown, John, Iborra, Francisco, Orntoft, Torben, Thykjaer, Thomas, Maltby, Edna, Smith, Kath, Dawud, Raed Abu, Jones, Mark, Matin, Maryam, Gokhale, Paul, Draper, Jonathan, Andrews, Peter W.

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Screening ethnically diverse human embryonic stem cells identifies a chromosome 20 minimal amplicon conferring growth advantage von Amps, Katherine, Andrews, Peter W, Anyfantis, George, Armstrong, Lyle, Avery, Stuart, Baharvand, Hossein, Baker, Julie, Baker, Duncan, Munoz, Maria B, Beil, Stephen, Benvenisty, Nissim, Ben-Yosef, Dalit, Biancotti, Juan-Carlos, Bosman, Alexis, Brena, Romulo Martin, Brison, Daniel, Caisander, Gunilla, Camarasa, María V, Chen, Jieming, Chiao, Eric, Choi, Young Min, Choo, Andre B H, Collins, Daniel, Colman, Alan, Crook, Jeremy M, Daley, George Q, Dalton, Anne, De Sousa, Paul A, Denning, Chris, Downie, Janet, Dvorak, Petr, Montgomery, Karen D, Feki, Anis, Ford, Angela, Fox, Victoria, Fraga, Ana M, Frumkin, Tzvia, Ge, Lin, Gokhale, Paul J, Golan-Lev, Tamar, Gourabi, Hamid, Gropp, Michal, Lu, Guangxiu, Hampl, Ales, Harron, Katie, Healy, Lyn, Herath, Wishva, Holm, Frida, Hovatta, Outi, Hyllner, Johan, Inamdar, Maneesha S, Irwanto, Astrid Kresentia, Ishii, Tetsuya, Jaconi, Marisa, Jin, Ying, Kimber, Susan, Kiselev, Sergey, Knowles, Barbara B, Kopper, Oded, Kukharenko, Valeri, Kuliev, Anver, Lagarkova, Maria A, Laird, Peter W, Lako, Majlinda, Laslett, Andrew L, Lavon, Neta, Lee, Dong Ryul, Lee, Jeoung Eun, Li, Chunliang, Lim, Linda S, Ludwig, Tenneille E, Ma, Yu, Maltby, Edna, Mateizel, Ileana, Mayshar, Yoav, Mileikovsky, Maria, Minger, Stephen L, Miyazaki, Takamichi, Moon, Shin Yong, Moore, Harry, Mummery, Christine, Nagy, Andras, Nakatsuji, Norio, Narwani, Kavita, Oh, Steve K W, Oh, Sun Kyung, Olson, Cia, Otonkoski, Timo, Pan, Fei, Park, In-Hyun, Pells, Steve, Pera, Martin F, Pereira, Lygia V, Qi, Ouyang, Raj, Grace Selva, Reubinoff, Benjamin, Robins, Alan, Robson, Paul, Rossant, Janet, Salekdeh, Ghasem H

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Cancer Incidence and Mortality in Men with Klinefelter Syndrome: A Cohort Study von Swerdlow, Anthony J., Schoemaker, Minouk J., Higgins, Craig D., Wright, Alan F., Jacobs, Patricia A.

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Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein von Sarafidou, Theologia, Kahl, Christina, Martinez-Garay, Isabel, Mangelsdorf, Marie, Gesk, Stefan, Baker, Elizabeth, Kokkinaki, Maria, Talley, Polly, Maltby, Edna L., French, Lisa, Harder, Lana, Hinzmann, Bernd, Nobile, Carlo, Richkind, Kathy, Finnis, Merran, Deloukas, Panagiotis, Sutherland, Grant R., Kutsche, Kerstin, Moschonas, Nicholas K., Siebert, Reiner, Gécz, Jozef

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Molecular Abnormalities in Pediatric Barrett Esophagus: Can We Test for Potential of Neoplastic Progression? von Maltby, Edna L., Dyson, Michael J., Wheeler, Mark R., Thomson, Mike, Sethuraman, Chitra, Cohen, Marta C.

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Prenatal diagnosis/Authors' reply von Caroline Mackie Ogilvie, Flinter, Frances, Caine, Allan, Maltby, Edna L

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Prenatal diagnosis – Authors' reply von Caine, Allan, Maltby, Edna L, Anthony Parkin, C, Waters, Jonathan J, Crolla, John A

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Prenatal diagnosis von Mackie Ogilvie, Caroline, Flinter, Frances

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Meningiomas, dicentric chromosomes, gliomas, and telomerase activity von Carroll, Thomas, Maltby, Edna, Brock, Ian, Royds, Janice, Timperley, Walter, Jellinek, David

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TMPRSS2 fusions in prostate cancer von Cross, Simon S, Rehman, Ishtiaq, Hamdy, Freddie.C, Sethuraman, Chitra, Goepel, John.R, Maltby, Edna

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Xp21 muscular dystrophy due to X chromosome inversion von BAXTER, P. S, MALTBY, E. L, QUARRELL, O

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Duplication involving band 4q32 with minimal clinical effect von Maltby, Edna L., Barnes, Islay C.S., Bennett, Christopher P.

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Cytogenetic studies in 50 meningiomas von Maltby, Edna L., Ironside, James W., Battersby, Robert D.E.

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