Flow Cytogenetics

por Carter, N P
Publicado 1991

CD3(-) Leukocytes Present in the Human Uterus During Early Placentation: Phenotypic and Morphologic Characterization of the CD56(++) Population

por King, Ashley, Balendran, Nalini, Wooding, P., Carter, N. P., Loke, Y. W.
Publicado 1991

Expression profiling of single cells using 3 prime end amplification (TPEA) PCR.

por Dixon, A K, Richardson, P J, Lee, K, Carter, N P, Freeman, T C
Publicado 1998

Molecular analysis of three patients with interstitial deletions of chromosome band 14q31.

por Byth, B C, Costa, M T, Teshima, I E, Wilson, W G, Carter, N P, Cox, D W
Publicado 1995

Coincidence painting: a rapid method for cloning region specific DNA sequences.

por Bailey, D M, Carter, N P, de Vos, D, Leversha, M A, Perryman, M T, Ferguson-Smith, M A
Publicado 1993

Tetrasomy 15q: two marker chromosomes with no detectable alpha-satellite DNA.

por Blennow, E., Telenius, H., de Vos, D., Larsson, C., Henriksson, P., Johansson, O., Carter, N. P., Nordenskjöld, M.
Publicado 1994

Analysis of four microsatellite markers on the long arm of chromosome 9 by meiotic recombination in flow-sorted single sperm.

por Furlong, R A, Goudie, D R, Carter, N P, Lyall, J E, Affara, N A, Ferguson-Smith, M A
Publicado 1993

Prenatal diagnosis from maternal blood: simultaneous immunophenotyping and FISH of fetal nucleated erythrocytes isolated by negative magnetic cell sorting.

por Zheng, Y L, Carter, N P, Price, C M, Colman, S M, Milton, P J, Hackett, G A, Greaves, M F, Ferguson-Smith, M A
Publicado 1993

Kallmann syndrome in a boy with a t(1;10) translocation detected by reverse chromosome painting.

por Schinzel, A, Lorda-Sanchez, I, Binkert, F, Carter, N P, Bebb, C E, Ferguson-Smith, M A, Eiholzer, U, Zachmann, M, Robinson, W P
Publicado 1995

Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics.

por Carter, N P, Ferguson-Smith, M A, Perryman, M T, Telenius, H, Pelmear, A H, Leversha, M A, Glancy, M T, Wood, S L, Cook, K, Dyson, H M
Publicado 1992

Prenatal detection of unbalanced chromosomal rearrangements by array CGH

por Rickman, L, Fiegler, H, Shaw‐Smith, C, Nash, R, Cirigliano, V, Voglino, G, Ng, B L, Scott, C, Whittaker, J, Adinolfi, M, Carter, N P, Bobrow, M
Publicado 2006

Constitutional Haploinsufficiency of Tumor Suppressor Genes in Mentally Retarded Patients With Microdeletions in 17p13.1

por Krepischi-Santos, A.C.V., Rajan, D., Temple, I.K., Shrubb, V., Crolla, J.A., Huang, S., Beal, S., Otto, P.A., Carter, N.P., Vianna-Morgante, A.M., Rosenberg, C.
Publicado 2009

Ultra‐high resolution array painting facilitates breakpoint sequencing

por Gribble, S M, Kalaitzopoulos, D, Burford, D C, Prigmore, E, Selzer, R R, Ng, B L, Matthews, N S W, Porter, K M, Curley, R, Lindsay, S J, Baptista, J, Richmond, T A, Carter, N P
Publicado 2007

Array‐based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

por Jacquemont, M‐L, Sanlaville, D, Redon, R, Raoul, O, Cormier‐Daire, V, Lyonnet, S, Amiel, J, Merrer, M Le, Heron, D, de Blois, M‐C, Prieur, M, Vekemans, M, Carter, N P, Munnich, A, Colleaux, L, Philippe, A
Publicado 2006

Array‐CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents

por Rosenberg, C, Knijnenburg, J, Bakker, E, Vianna‐Morgante, A M, Sloos, W, Otto, P A, Kriek, M, Hansson, K, Krepischi‐Santos, A C V, Fiegler, H, Carter, N P, Bijlsma, E K, van Haeringen, A, Szuhai, K, Tanke, H J
Publicado 2006

Integration of cytogenetic landmarks into the draft sequence of the human genome

por BAC Resource Consortium, The, Cheung, V. G., Nowak, N., Jang, W., Kirsch, I. R., Zhao, S., Chen, X.-N., Furey, T. S., Kim, U.-J., Kuo, W.-L., Olivier, M., Conroy, J., Kasprzyk, A., Massa, H., Yonescu, R., Sait, S., Thoreen, C., Snijders, A., Lemyre, E., Bailey, J. A., Bruzel, A., Burrill, W. D., Clegg, S. M., Collins, S., Dhami, P., Friedman, C., Han, C. S., Herrick, S., Lee, J., Ligon, A. H., Lowry, S., Morley, M., Narasimhan, S., Osoegawa, K., Peng, Z., Plajzer-Frick, I., Quade, B. J., Scott, D., Sirotkin, K., Thorpe, A. A., Gray, J. W., Hudson, J., Pinkel, D., Ried, T., Rowen, L., Shen-Ong, G. L., Strausberg, R. L., Birney, E., Callen, D. F., Cheng, J.-F., Cox, D. R., Doggett, N. A., Carter, N. P., Eichler, E. E., Haussler, D., Korenberg, J. R., Morton, C. C., Albertson, D., Schuler, G., de Jong, P. J., Trask, B. J.
Publicado en Nature (2001)

The DNA sequence and analysis of human chromosome 13

por Dunham, A., Matthews, L. H., Burton, J., Ashurst, J. L., Howe, K. L., Ashcroft, K. J., Beare, D. M., Burford, D. C., Hunt, S. E., Griffiths-Jones, S., Jones, M. C., Keenan, S. J., Oliver, K., Scott, C. E., Ainscough, R., Almeida, J. P., Ambrose, K. D., Andrews, D. T., Ashwell, R. I. S., Babbage, A. K., Bagguley, C. L., Bailey, J., Bannerjee, R., Barlow, K. F., Bates, K., Beasley, H., Bird, C. P., Bray-Allen, S., Brown, A. J., Brown, J. Y., Burrill, W., Carder, C., Carter, N. P., Chapman, J. C., Clamp, M. E., Clark, S. Y., Clarke, G., Clee, C. M., Clegg, S. C. M., Cobley, V., Collins, J. E., Corby, N., Coville, G. J., Deloukas, P., Dhami, P., Dunham, I., Dunn, M., Earthrowl, M. E., Ellington, A. G., Faulkner, L., Frankish, A. G., Frankland, J., French, L., Garner, P., Garnett, J., Gilbert, J. G. R., Gilson, C. J., Ghori, J., Grafham, D. V., Gribble, S. M., Griffiths, C., Hall, R. E., Hammond, S., Harley, J. L., Hart, E. A., Heath, P. D., Howden, P. J., Huckle, E. J., Hunt, P. J., Hunt, A. R., Johnson, C., Johnson, D., Kay, M., Kimberley, A. M., King, A., Laird, G. K., Langford, C. J., Lawlor, S., Leongamornlert, D. A., Lloyd, D. M., Lloyd, C., Loveland, J. E., Lovell, J., Martin, S., Mashreghi-Mohammadi, M., McLaren, S. J., McMurray, A., Milne, S., Moore, M. J. F., Nickerson, T., Palmer, S. A., Pearce, A. V., Peck, A. I., Pelan, S., Phillimore, B., Porter, K. M., Rice, C. M., Searle, S., Sehra, H. K., Shownkeen, R., Skuce, C. D., Smith, M., Steward, C. A., Sycamore, N., Tester, J., Thomas, D. W., Tracey, A., Tromans, A., Tubby, B., Wall, M., Wallis, J. M., West, A. P., Whitehead, S. L., Willey, D. L., Wilming, L., Wray, P. W., Wright, M. W., Young, L., Coulson, A., Durbin, R., Hubbard, T., Sulston, J. E., Beck, S., Bentley, D. R., Rogers, J., Ross, M. T.
Publicado 2004

DNA sequence and analysis of human chromosome 9

por Humphray, S. J., Oliver, K., Hunt, A. R., Plumb, R. W., Loveland, J. E., Howe, K. L., Andrews, T. D., Searle, S., Hunt, S. E., Scott, C. E., Jones, M. C., Ainscough, R., Almeida, J. P., Ambrose, K. D., Ashwell, R. I. S., Babbage, A. K., Babbage, S., Bagguley, C. L., Bailey, J., Banerjee, R., Barker, D. J., Barlow, K. F., Bates, K., Beasley, H., Beasley, O., Bird, C. P., Bray-Allen, S., Brown, A. J., Brown, J. Y., Burford, D., Burrill, W., Burton, J., Carder, C., Carter, N. P., Chapman, J. C., Chen, Y., Clarke, G., Clark, S. Y., Clee, C. M., Clegg, S., Collier, R. E., Corby, N., Crosier, M., Cummings, A. T., Davies, J., Dhami, P., Dunn, M., Dutta, I., Dyer, L. W., Earthrowl, M. E., Faulkner, L., Fleming, C. J., Frankish, A., Frankland, J. A., French, L., Fricker, D. G., Garner, P., Garnett, J., Ghori, J., Gilbert, J. G. R., Glison, C., Grafham, D. V., Gribble, S., Griffiths, C., Griffiths-Jones, S., Grocock, R., Guy, J., Hall, R. E., Hammond, S., Harley, J. L., Harrison, E. S. I., Hart, E. A., Heath, P. D., Henderson, C. D., Hopkins, B. L., Howard, P. J., Howden, P. J., Huckle, E., Johnson, C., Johnson, D., Joy, A. A., Kay, M., Keenan, S., Kershaw, J. K., Kimberley, A. M., King, A., Knights, A., Laird, G. K., Langford, C., Lawlor, S., Leongamornlert, D. A., Leversha, M., Lloyd, C., Lloyd, D. M., Lovell, J., Martin, S., Mashreghi-Mohammadi, M., Matthews, L., McLaren, S., McLay, K. E., McMurray, A., Milne, S., Nickerson, T., Nisbett, J., Nordsiek, G., Pearce, A. V., Peck, A. I., Porter, K. M., Pandian, R., Pelan, S., Phillimore, B., Povey, S., Ramsey, Y., Rand, V., Scharfe, M., Sehra, H. K., Shownkeen, R., Sims, S. K., Skuce, C. D., Smith, M., Steward, C. A., Swarbreck, D., Sycamore, N., Tester, J., Thorpe, A., Tracey, A., Tromans, A., Thomas, D. W., Wall, M., Wallis, J. M., West, A. P., Whitehead, S. L., Willey, D. L., Williams, S. A., Wilming, L., Wray, P. W., Young, L., Ashurst, J. L., Coulson, A., Blöcker, H., Durbin, R., Sulston, J. E., Hubbard, T., Jackson, M. J., Bentley, D. R., Beck, S., Rogers, J., Dunham, I.
Publicado 2004