Flow Cytogenetics

Por Carter, N P
Publicado em 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 em 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 em 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 em 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 em 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 em 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 em 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 em 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 em 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 em 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 em 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 em 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 em 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 em 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 em 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 no 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 em 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 em 2004