Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome von van Bueren, Kelly Lammerts, Papangeli, Irinna, Rochais, Francesca, Pearce, Kerra, Roberts, Catherine, Calmont, Amelie, Szumska, Dorota, Kelly, Robert G., Bhattacharya, Shoumo, Scambler, Peter J.

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Molecular study of 33 families with Fraser syndrome new data and mutation review von van Haelst, M.M., Maiburg, M., Baujat, G., Jadeja, S., Monti, E., Bland, E., Pearce, K., Hennekam, R.C., Scambler, P.J.

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Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus von Scambler, P.J, Kelly, D, Lindsay, E, Williamson, R, Goldberg, R, Shprintzen, R, Wilson, D.I, Goodship, J.A, Cross, I.E, Burn, J

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Severe digital abnormalities in a patient heterozygous for both a novel missense mutation in HOXD13 and a polyalanine tract expansion in HOXA13 von Debeer, P, Bacchelli, C, Scambler, P J, De Smet, L, Fryns, J-P, Goodman, F R

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Deletions within chromosome 22q11 in familial congenital heart disease von Wilson, D.I, Goodship, J.A, Burn, J, Cross, I.E, Scambler, P.J

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Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome von Carey, A H, Kelly, D, Halford, S, Wadey, R, Wilson, D, Goodship, J, Burn, J, Paul, T, Sharkey, A, Dumanski, J

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Genotype-Phenotype Correlation of Mutations in Fras1 with Fraser Syndrome Patients von Chu, C.S., Rabinowitz, Y.S., Scambler, P.J., Graham, J.M.

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Molecular Cytogenetic Characterization of the DiGeorge Syndrome Region Using Fluorescence in Situ Hybridization von Lindsay, Elizabeth A., Halford, Stephanie, Wadey, Roy, Scambler, Peter J., Baldini, Antonio

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A prospective cytogenetic study of 36 cases of DiGeorge syndrome von WILSON, D. I, CROSS, I. E, WOLSTENHOLME, J, GOODSHIP, J. A, BROW, J, SCAMBLER, P. J, BAIN, H. H, TAYLOR, J. F., WALSH, K, BANKIER, A, BURN, J

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A locus for asphyxiating thoracic dystrophy, ATD, maps to chromosome 15q 13 von MORGAN, N. V, BACCHELLI, C, KELLY, D. A, TREMBATH, R. C, SCAMBLER, P. J, MAHER, E. R, GOODMAN, F. R, JOHNSON, C. A, GISSEN, P, MORTON, J, FERRERO, G. B, SILENGO, M, LABRUNE, P, CASTEELS, I, HALL, C, COX, P

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Localization of 27 DNA markers to the region of human chromosome 22q11-pter deleted in patients with the DiGeorge syndrome and duplicated in the der22 syndrome von Carey, A.H., Roach, S., Willamson, R., Dumanski, J.P., Nordenskiold, M., Collins, V.P., Rouleau, G., Blin, N., Jalbert, P., Scambler, P.J.

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Mapping of the Tuple1 Gene to Mouse Chromosome 16A-B1 von Mattei, Marie-Genevieve, Halford, Stephanie, Scambler, Peter J.

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Patterns of polymorphism and linkage disequilibrium for cystic fibrosis von Estivill, X., Scambler, P.J., Wainwright, B.J., Hawley, K., Frederick, P., Schwartz, M., Baiget, M., Kere, J., Williamson, R., Farrall, M.

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Supplementary Material for: An FDA-Approved Drug Screen for Compounds Influencing Craniofacial Skeletal Development and Craniosynostosis von Seda, M., Geerlings, M., Lim, P., Jeyabalan-Srikaran, J., Cichon, A.-C., Scambler, P.J., Beales, P.L., Hernandez-Hernandez, V., Stoker, A.W., Jenkins, D.

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Characterisation of a short interspersed repeat (Mermaid) that has family members on human chromosome 21 and elsewhere in the human genome von HOYLE, J, YULUG, I. G, JOHNSTONE, K, SCAMBLER, P. J, FISHER, E. M. C

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Isolation of a further anonymous informative DNA sequence from chromosome seven closely linked to cystic flbrosis von Scambler, P.J., Wainwright, B.J., Walson, E., Bates, G., Bell, G., Williamson, R., Farrall, M.

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A dual FISH assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci von Berend, S.A., Holmes, R.K., Craigen, W.J., Spikes, A.S., Kashork, C.D., Wu, J.M., Daw, S.C., Scambler, P.J., Shaffer, L.G.

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Isolation of anonymous DNA markers for human chromosome 22q11 from a flow-sorted library, and mapping using hybrids from patients with DiGeorge syndrome von SHARKEY, A. M, MCLAREN, L, CARROLL, M, FANTES, J, GREEN, D, WILSON, D, SCAMBLER, P. J, EVANS, H. J

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Isolation and mapping of a polymorphic DNA sequence pXH3 on chromosome X [DXS235] von ESTIVILL, X, SCAMBLER, P. J

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An anonymous DNA probe (NL32) recognises a MspI polymorphism on human chromosome 1 [D1S84] von Lench, N J, Scambler, P J

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