A homeobox gene, HLXB9 , is the major locus for dominantly inherited sacral agenesis
Strachan, Tom, Ross, Alison J, Ruiz-Perez, Victor, Wang, Yiming, Hagan, Donna-Marie, Scherer, Steve, Lynch, Sally A, Lindsay, Susan, Custard, Emily, Belloni, Elena, Wilson, David I, Wadey, Roy, Goodman, Frances, Orstavik, Karen Helene, Monclair, Tom, Robson, Steve, Reardon, William, Burn, John, Scambler, Pete
Published in Nature genetics (01.12.1998)
Published in Nature genetics (01.12.1998)
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Frequent RASSF1A tumour suppressor gene promoter methylation in Wilms' tumour and colorectal cancer
Wagner, Kate J, Cooper, Wendy N, Grundy, Richard G, Caldwell, Germaine, Jones, Carolyn, Wadey, Roy B, Morton, Dion, Schofield, Paul N, Reik, Wolf, Latif, Farida, Maher, Eamonn R
Published in Oncogene (17.10.2002)
Published in Oncogene (17.10.2002)
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Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome
Wadey, R, Daw, S, Taylor, C, Atif, U, Kamath, S, Halford, S, O'Donnell, H, Wilson, D, Goodship, J, Burn, J
Published in Human molecular genetics (01.06.1995)
Published in Human molecular genetics (01.06.1995)
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Journal Article
Isolation of a gene expressed during early embryogenesis from the region of 22q11 commonly deleted in DiGeorge syndrome
Halford, S, Wilson, D I, Daw, S C, Roberts, C, Wadey, R, Kamath, S, Wickremasinghe, A, Burn, J, Goodship, J, Mattei, M G
Published in Human molecular genetics (01.10.1993)
Published in Human molecular genetics (01.10.1993)
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Journal Article
Direct selection of conserved cDNAs from the DiGeorge critical region: isolation of a novel CDC45-like gene
McKie, J M, Wadey, R B, Sutherland, H F, Taylor, C L, Scambler, P J
Published in Genome research (01.08.1998)
Published in Genome research (01.08.1998)
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Journal Article
Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease
Halford, S, Wadey, R, Roberts, C, Daw, S C, Whiting, J A, O'Donnell, H, Dunham, I, Bentley, D, Lindsay, E, Baldini, A
Published in Human molecular genetics (01.12.1993)
Published in Human molecular genetics (01.12.1993)
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Journal Article
Possible role for COMT in psychosis associated with velo-cardio-facial syndrome
Dunham, Ian, Collins, John, Wadey, Roy, Scambler, Peter
Published in The Lancet (British edition) (28.11.1992)
Published in The Lancet (British edition) (28.11.1992)
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Mutations of UFD1L Are Not Responsible for the Majority of Cases of DiGeorge Syndrome/Velocardiofacial Syndrome without Deletions within Chromosome 22q11
Wadey, Roy, McKie, Judith, Papapetrou, Charalambos, Sutherland, Helen, Lohman, Frans, Osinga, Jan, Frohn, Ingrid, Hofstra, Robert, Meijers, Carel, Amati, Francesca, Conti, Emanuela, Pizzuti, Antonio, Dallapiccola, Bruno, Novelli, Giuseppe, Scambler, Peter
Published in American journal of human genetics (01.07.1999)
Published in American journal of human genetics (01.07.1999)
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Journal Article
Loss of heterozygosity in Wilms' tumour involves two distinct regions of chromosome 11
Wadey, R B, Pal, N, Buckle, B, Yeomans, E, Pritchard, J, Cowell, J K
Published in Oncogene (01.06.1990)
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Published in Oncogene (01.06.1990)
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Preferential loss of maternal alleles in sporadic Wilms' tumour
Pal, N, Wadey, R B, Buckle, B, Yeomans, E, Pritchard, J, Cowell, J K
Published in Oncogene (01.11.1990)
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Published in Oncogene (01.11.1990)
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Structural rearrangements of the WT1 gene in Wilms' tumour cells
Cowell, J K, Wadey, R B, Haber, D A, Call, K M, Housman, D E, Pritchard, J
Published in Oncogene (01.04.1991)
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Published in Oncogene (01.04.1991)
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Cloning and mapping of murine Dgcr2 and its homology to the Sez-12 seizure-related protein
Taylor, C, Wadey, R, O'Donnell, H, Roberts, C, Mattei, M G, Kimber, W L, Wynshaw-Boris, A, Scambler, P J
Published in Mammalian genome (01.05.1997)
Published in Mammalian genome (01.05.1997)
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