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212 results

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Page 1
Prenatal detection of unbalanced chromosomal rearrangements by array CGH.
Rickman L, Fiegler H, Shaw-Smith C, Nash R, Cirigliano V, Voglino G, Ng BL, Scott C, Whittaker J, Adinolfi M, Carter NP, Bobrow M. Rickman L, et al. Among authors: carter np. J Med Genet. 2006 Apr;43(4):353-61. doi: 10.1136/jmg.2005.037648. Epub 2005 Sep 30. J Med Genet. 2006. PMID: 16199537 Free PMC article.
Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features.
Shaw-Smith C, Redon R, Rickman L, Rio M, Willatt L, Fiegler H, Firth H, Sanlaville D, Winter R, Colleaux L, Bobrow M, Carter NP. Shaw-Smith C, et al. Among authors: carter np. J Med Genet. 2004 Apr;41(4):241-8. doi: 10.1136/jmg.2003.017731. J Med Genet. 2004. PMID: 15060094 Free PMC article.
The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes.
Gribble SM, Prigmore E, Burford DC, Porter KM, Ng BL, Douglas EJ, Fiegler H, Carr P, Kalaitzopoulos D, Clegg S, Sandstrom R, Temple IK, Youings SA, Thomas NS, Dennis NR, Jacobs PA, Crolla JA, Carter NP. Gribble SM, et al. Among authors: carter np. J Med Genet. 2005 Jan;42(1):8-16. doi: 10.1136/jmg.2004.024141. J Med Genet. 2005. PMID: 15635069 Free PMC article.
Prenatal diagnosis by array-CGH.
Rickman L, Fiegler H, Carter NP, Bobrow M. Rickman L, et al. Among authors: carter np. Eur J Med Genet. 2005 Jul-Sep;48(3):232-40. doi: 10.1016/j.ejmg.2005.03.003. Eur J Med Genet. 2005. PMID: 16179219 Review.
Ultra-high resolution array painting facilitates breakpoint sequencing.
Gribble SM, Kalaitzopoulos D, Burford DC, Prigmore E, Selzer RR, Ng BL, Matthews NS, Porter KM, Curley R, Lindsay SJ, Baptista J, Richmond TA, Carter NP. Gribble SM, et al. Among authors: carter np. J Med Genet. 2007 Jan;44(1):51-8. doi: 10.1136/jmg.2006.044909. Epub 2006 Sep 13. J Med Genet. 2007. PMID: 16971479 Free PMC article.
High resolution array-CGH analysis of single cells.
Fiegler H, Geigl JB, Langer S, Rigler D, Porter K, Unger K, Carter NP, Speicher MR. Fiegler H, et al. Among authors: carter np. Nucleic Acids Res. 2007;35(3):e15. doi: 10.1093/nar/gkl1030. Epub 2006 Dec 18. Nucleic Acids Res. 2007. PMID: 17178751 Free PMC article.
Applications of combined DNA microarray and chromosome sorting technologies.
Gribble SM, Fiegler H, Burford DC, Prigmore E, Yang F, Carr P, Ng BL, Sun T, Kamberov ES, Makarov VL, Langmore JP, Carter NP. Gribble SM, et al. Among authors: carter np. Chromosome Res. 2004;12(1):35-43. doi: 10.1023/b:chro.0000009325.69828.83. Chromosome Res. 2004. PMID: 14984100
Tiling path resolution mapping of constitutional 1p36 deletions by array-CGH: contiguous gene deletion or "deletion with positional effect" syndrome?
Redon R, Rio M, Gregory SG, Cooper RA, Fiegler H, Sanlaville D, Banerjee R, Scott C, Carr P, Langford C, Cormier-Daire V, Munnich A, Carter NP, Colleaux L. Redon R, et al. Among authors: carter np. J Med Genet. 2005 Feb;42(2):166-71. doi: 10.1136/jmg.2004.023861. J Med Genet. 2005. PMID: 15689456 Free PMC article. No abstract available.
212 results