Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence von Vazquez, Marie-Paule, Fantes, Judy A, Vekemans, Michel, Holder-Espinasse, Muriel, Gordon, Christopher T, Kilpatrick, Nicky, Perry, Paul, Heaney, Simon, Thomas, Sophie, Ayuso, Carmen, Ramsay, Jacqueline, Lees, Melissa M, Crollius, Hugues Roest, Farlie, Peter G, Abadie, Véronique, Temple, I Karen, Lyonnet, Stanislas, Amiel, Jeanne, Fisher, Malcolm, Thomas, Paul, Kleinjan, Dirk-Jan, Etchevers, Heather C, Benko, Sabina, Jamshidi, Negar, Munnich, Arnold, Pelet, Anna, Essafi, Abdelkader, McBride, David, FitzPatrick, David R, Golzio, Christelle, Picard, Arnaud, Hastie, Nicholas D

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Mutations in SOX2 cause anophthalmia-esophageal-genital (AEG) syndrome von Williamson, Kathleen A., Hever, Ann M., Rainger, Joe, Rogers, R. Curtis, Magee, Alex, Fiedler, Zdenek, Keng, Wee Teik, Sharkey, Freddie H., McGill, Niolette, Hill, Clare J., Schneider, Adele, Messina, Mario, Turnpenny, Peter D., Fantes, Judy A., van Heyningen, Veronica, FitzPatrick, David R.

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Identification of SATB2 as the cleft palate gene on 2q32–q33 von FitzPatrick, David R., Carr, Ian M., McLaren, Lorna, Leek, Jack P., Wightman, Patrick, Williamson, Kathy, Gautier, Philippe, McGill, Niolette, Hayward, Caroline, Firth, Helen, Markham, Alex F., Fantes, Judy A., Bonthron, David T.

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FISH Mapping of De Novo Apparently Balanced Chromosome Rearrangements Identifies Characteristics Associated with Phenotypic Abnormality von Fantes, J.A., Boland, E., Ramsay, J., Donnai, D., Splitt, M., Goodship, J.A., Stewart, H., Whiteford, M., Gautier, P., Harewood, L., Holloway, S., Sharkey, F., Maher, E., van Heyningen, V., Clayton-Smith, J., Fitzpatrick, D.R., Black, G.C.M.

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Large Genomic Duplicons Map to Sites of Instability in the Prader-Willi/Angelman Syndrome Chromosome Region (15q11–q13) von Christian, Susan L., Fantes, Judy A., Mewborn, Stephanie K., Huang, Bing, Ledbetter, David H.

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Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14 von Ungaro, Paola, Christian, Susan L, Fantes, Judy A, Mutirangura, Apiwat, Black, Susan, Reynolds, James, Malcolm, Sue, Dobyns, William B, Ledbetter, David H

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Variegated Transgene Expression in Mouse Mammary Gland is Determined by the Transgene Integration Locus von Dobie, Kenneth W., Lee, Muriel, Fantes, Judith A., Graham, Elizabeth, Clark, A. John, Springbett, Anthea, Lathe, Richard, McClenaghan, Margaret

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The Evolutionary Origin of Human Subtelomeric Homologies—or Where the Ends Begin von Martin, Christa Lese, Wong, Andrew, Gross, Alyssa, Chung, June, Fantes, Judy A., Ledbetter, David H.

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Organisation of the pericentromeric region of chromosome 15: at least four partial gene copies are amplified in patients with a proximal duplication of 15q von Fantes, J A, Mewborn, S K, Lese, C M, Hedrick, J, Brown, R L, Dyomin, V, Chaganti, R S K, Christian, S L, Ledbetter, D H

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APC mutation analysis by chemical cleavage of mismatch and a protein truncation assay in familial adenomatous polyposis von Prosser, J, Condie, A, Wright, M, Horn, JM, Fantes, JA, Wyllie, AH, Dunlop, MG

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Mutations in SOX2 cause anophthalmia–esophageal–genital (AEG) syndrome von Williamson, Kathleen A., Hever, Ann M., Rainger, Joe, Rogers, R. Curtis, Magee, Alex, Fiedler, Zdenek, Keng, Wee Teik, Sharkey, Freddie H., McGill, Niolette, Hill, Clare J., Schneider, Adele, Messina, Mario, Turnpenny, Peter D., Fantes, Judy A., van Heyningen, Veronica, FitzPatrick, David R.

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Submicroscopic deletions at the WAGR locus, revealed by nonradioactive in situ hybridization von FANTES, J. A, BICKMORE, W. A, FLETCHER, J. M, BALLESTA, F, HANSON, M, VAN HEYNINGEN, V

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Characterization of physical gap sizes at human telomeres von Lese, C M, Fantes, J A, Riethman, H C, Ledbetter, D H

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A high-resolution integrated physical, cytogenetic, and genetic map of human chromosome 11: distal p13 to proximal p15.1 von Fantes, Judy A., Oghene, Kathy, Boyle, Shelagh, Danes, Sarah, Fletcher, Judy M., Bruford, Elspeth A., Williamson, Kathy, Seawright, Anne, Schedl, Andreas, Hanson, Isabel, Zehetner, Günther, Bhogal, Ranjit, Lehrach, Hans, Gregory, Simon, Williams, Jon, Little, Peter F.R., Sellar, Grant C., Hoovers, Jan, Mannens, Marcel, Weissenbach, Jean, Junien, Claudine, van Heyningen, Veronica, Bickmore, Wendy A.

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A 6.9-Mb High-Resolution BAC/PAC Contig of Human 4p15.3–p16.1, a Candidate Region for Bipolar Affective Disorder von Evans, Kathryn L., Le Hellard, Stephanie, Morris, Stewart W., Lawson, Diane, Whitton, Claire, Semple, Colin A.M., Fantes, Judith A., Torrance, Helen S., Malloy, M.Pat, Maule, John C., Humphray, Sean J., Ross, Mark T., Bentley, David R., Muir, Walter J., Blackwood, Douglas H.R., Porteous, David J.

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The Human Serum Amyloid A Protein (SAA) Superfamily Gene Cluster: Mapping to Chromosome 11p15.1 by Physical and Genetic Linkage Analysis von Sellar, Grant C., Jordan, Siobhán A., Bickmore, Wendy A., Fantes, Judy A., van Heyningen, Veronica, Whitehead, Alexander S.

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Isolation of BAC clones spanning the Xq22.3 translocation breakpoint in a lissencephaly patient with a de novo X;2 translocation von Matsumoto, N, Pilz, D T, Fantes, J A, Kittikamron, K, Ledbetter, D H

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Co-localization of the ketohexokinase and glucokinase regulator genes to a 500-kb region of chromosome 2p23 von Hayward, B E, Fantes, J A, Warner, J P, Intody, S, Leek, J P, Markham, A F, Bonthron, D T

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Molecular Analysis of Chromosome 11 Deletions in Aniridia-Wilms Tumor Syndrome von Van Heyningen, Veronica, Boyd, Patricia A., Seawright, Anne, Fletcher, Judy M., Fantes, Judy A., Buckton, Karen E., Spowart, George, Porteous, David J., Hill, Robert E., Newton, Marjorie S., Hastie, Nicholas D.

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Application of Automation to the Detection of Radiation Damage Using FISH Technology von Fantes, J.A., Green, D.K., Hill, W., Stark, M.H., Gordon, J.M., Piper, J.

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