Mapping of the Tuple1 gene to mouse chromosome 16A-B1. by Mattei, MG, Halford, S, Scambler, P

A novel C2H2 zinc-finger protein gene (ZNF160) maps to human chromosome 19q13.3-q13.4. by Halford, S, Mattei, MG, Daw, S, Scambler, P

A rapid and sensitive assay for quantification of siRNA efficiency and specificity. by Smart, N, Scambler, P, Riley, P

Cloning and developmental expression analysis of chick Hira (Chira), a candidate gene for DiGeorge syndrome. by Roberts, C, Daw, S, Halford, S, Scambler, P

Molecular cytogenetic characterization of the DiGeorge syndrome region using fluorescence in situ hybridization. by Lindsay, E, Halford, S, Wadey, R, Scambler, P, Baldini, A

Low-copy-number repeat sequences flank the DiGeorge/velo-cardio-facial syndrome loci at 22q11. by Halford, S, Lindsay, E, Nayudu, M, Carey, A, Baldini, A, Scambler, P

Modelling human microdeletion syndromes by chromosome engineering in mice by Shaw-Smith, C, Storer, M, Szumska, D, Scambler, P, Bhattacharya, S, Bradley, A

Dissecting the embryonic requirement of the Notch pathway gene, Hes1, in the context of DiGeorge syndrome by Papangeli, I, Van Bueren, K, Pearce, K, Roberts, C, Szumska, D, Bhattacharya, S, Scambler, P

Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridization. by Desmaze, C, Scambler, P, Prieur, M, Halford, S, Sidi, D, Le Deist, F, Aurias, A

HIC2 is a novel dosage-dependent regulator of cardiac development located within the distal 22q11 deletion syndrome region. by Dykes, I, van Bueren, K, Ashmore, R, Floss, T, Wurst, W, Szumska, D, Bhattacharya, S, Scambler, P

Isolation of a new marker and conserved sequences close to the DiGeorge syndrome marker HP500 (D22S134). by Wadey, R, Daw, S, Wickremasinghe, A, Roberts, C, Wilson, D, Goodship, J, Burn, J, Halford, S, Scambler, P

Targeted mutagenesis of the Hira gene results in gastrulation defects and patterning abnormalities of mesoendodermal derivatives prior to early embryonic lethality. by Roberts, C, Sutherland, H, Farmer, H, Kimber, W, Halford, S, Carey, A, Brickman, J, Wynshaw-Boris, A, Scambler, P

Cardiac phenotyping in ex vivo murine embryos using microMRI. by Cleary, J, Price, A, Thomas, D, Scambler, P, Kyriakopoulou, V, McCue, K, Schneider, J, Ordidge, R, Lythgoe, M

The representation of heart development in the gene ontology. by Khodiyar, V, Hill, D, Howe, D, Berardini, T, Tweedie, S, Talmud, P, Breckenridge, R, Bhattarcharya, S, Riley, P, Scambler, P, Lovering, R

Cloning the mouse homolog of the human cystic fibrosis transmembrane conductance regulator gene. by Tata, F, Stanier, P, Wicking, C, Halford, S, Kruyer, H, Lench, N, Scambler, P, Hansen, C, Braman, J, Williamson, R

22Q11 - PHYSICAL, COMPARATIVE AND DISEASE LOCUS MAPPING by Halford, S, Odonnell, H, Daw, S, Wadey, R, Raylor, K, Lindsay, E, Baldini, A, Collins, J, Dunham, I, Bentley, D, Scambler, P

Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome. by van Bueren, K, Papangeli, I, Rochais, F, Pearce, K, Roberts, C, Calmont, A, Szumska, D, Kelly, R, Bhattacharya, S, Scambler, P

Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome. by Sutherland, H, Wadey, R, McKie, J, Taylor, C, Atif, U, Johnstone, K, Halford, S, Kim, U, Goodship, J, Baldini, A, Scambler, P

MOLECULAR STUDIES OF MONOSOMY-22Q11 AND ITS CLINICAL CONSEQUENCES by Scambler, P, Halford, S, Wadey, R, Lindsay, E, Kelly, D, Wilson, D, Goodship, J, Burn, J, Goldberg, R, Shprintzen, R, Williamson, R, Carey, A

Identification of a new human catenin gene family member (ARVCF) from the region deleted in velo-cardio-facial syndrome. by Sirotkin, H, O'Donnell, H, DasGupta, R, Halford, S, St Jore, B, Puech, A, Parimoo, S, Morrow, B, Skoultchi, A, Weissman, S, Scambler, P, Kucherlapati, R