First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders von Mackay, Deborah, Bliek, Jet, Kagami, Masayo, Tenorio-Castano, Jair, Pereda, Arrate, Brioude, Frédéric, Netchine, Irène, Papingi, Dzhoy, de Franco, Elisa, Lever, Margaret, Sillibourne, Julie, Lombardi, Paola, Gaston, Véronique, Tauber, Maithé, Diene, Gwenaelle, Bieth, Eric, Fernandez, Luis, Nevado, Julian, Tümer, Zeynep, Riccio, Andrea, Maher, Eamonn R, Beygo, Jasmin, Tannorella, Pierpaola, Russo, Silvia, de Nanclares, Guiomar Perez, Temple, I. Karen, Ogata, Tsutomu, Lapunzina, Pablo, Eggermann, Thomas

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A patient with multilocus imprinting disturbance involving hypomethylation at 11p15 and 14q32, and phenotypic features of Beckwith‐Wiedemann and Temple syndromes von Grosvenor, Sarah E., Davies, Justin H., Lever, Margaret, Sillibourne, Julie, Mackay, Deborah J. G., Temple, I. Karen

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Identification of a de novo BRCA1 mutation in a woman with early onset bilateral breast cancer von Edwards, Emma, Yearwood, Catharina, Sillibourne, Julie, Baralle, Diana, Eccles, Diana

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Oculopharyngeal muscular dystrophy (opmd): analysis of the PABPN1 gene expansion sequence in 86 patients reveals 13 different expansion types and further evidence for unequal recom... von ROBINSON, David O, HAMMANS, Simon R, READ, Steven P, SILLIBOURNE, Julie

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Simultaneous MLPA-based multiplex point mutation and deletion analysis of the Dystrophin gene von BUNYAN, David J, SKINNER, Alison C, ASHTON, Emma J, SILLIBOURNE, Julie, BROWN, Tom, COLLINS, Amanda L, CROSS, Nicholas C. P, HARVEY, John F, ROBINSON, David O

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Mutation scanning by meltMADGE: validations using BRCA1 and LDLR, and demonstration of the potential to identify severe, moderate, silent, rare, and paucimorphic mutations in the g... von Alharbi, Khalid K, Aldahmesh, Mohammed A, Spanakis, Emmanuel, Haddad, Lema, Whittall, Roslyn A, Chen, Xiao-he, Rassoulian, Hamid, Smith, Matt J, Sillibourne, Julie, Ball, Nicola J, Graham, Nikki J, Briggs, Patricia J, Simpson, Iain A, Phillips, David I W, Lawlor, Deborah A, Ye, Shu, Humphries, Stephen E, Cooper, Cyrus, Smith, George Davey, Ebrahim, Shah, Eccles, Diana M, Day, Ian N M

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Oculopharyngeal muscular dystrophy von Robinson, David O, Hammans, Simon R, Read, Steven P, Sillibourne, Julie

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First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders von Mackay, Deborah, Bliek, Jet, Kagami, Masayo, Tenorio-Castano, Jair, Pereda, Arrate, Brioude, Frédéric, Netchine, Irène, Papingi, Dzhoy, de Franco, Elisa, Lever, Margaret, Sillibourne, Julie, Lombardi, Paola, Gaston, Véronique, Tauber, Maithé, Diene, Gwenaelle, Bieth, Eric, Fernandez, Luis, Nevado, Julian, Tümer, Zeynep, Riccio, Andrea, Maher, Eamonn R, Beygo, Jasmin, Tannorella, Pierpaola, Russo, Silvia, de Nanclares, Guiomar Perez, Temple, I Karen, Ogata, Tsutomu, Lapunzina, Pablo, Eggermann, Thomas

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First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders von Mackay, Deborah, Bliek, Jet, Kagami, Masayo, Tenorio-Castano, Jair, Pereda, Arrate, Brioude, Frédéric, Netchine, Irène, Papingi, Dzhoy, de Franco, Elisa, Lever, Margaret, Sillibourne, Julie, Lombardi, Paola, Gaston, Véronique, Tauber, Maithé, Diene, Gwenaelle, Bieth, Eric, Fernandez, Luis, Nevado, Julian, Tümer, Zeynep, Riccio, Andrea, Maher, Eamonn R, Beygo, Jasmin, Tannorella, Pierpaola, Russo, Silvia, de Nanclares, Guiomar Perez, Temple, I Karen, Ogata, Tsutomu, Lapunzina, Pablo, Eggermann, Thomas

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Quantification of Marek's disease virus in chicken lymphocytes using the polymerase chain reaction with fluorescence detection von Bumstead, Nat, Sillibourne, Julie, Rennie, Mike, Ross, Norman, Davison, Fred

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A patient with multilocus imprinting disturbance involving hypomethylation at 11p15 and 14q32, and phenotypic features of Beckwith-Wiedemann and Temple syndromes von Grosvenor, Sarah E, Davies, Justin H, Lever, Margaret, Sillibourne, Julie, Mackay, Deborah J G, Temple, I Karen

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