Knight S - Search Results

1

The use of telomere probes to investigate submicroscopic rearrangements associated with mental retardation.

Flint J, Knight S. Flint J, et al. Among authors: knight s. Curr Opin Genet Dev. 2003 Jun;13(3):310-6. doi: 10.1016/s0959-437x(03)00049-2. Curr Opin Genet Dev. 2003. PMID: 12787795

2

Segregation of FRAXE in a large family: clinical, psychometric, cytogenetic, and molecular data.

Hamel BC, Smits AP, de Graaff E, Smeets DF, Schoute F, Eussen BH, Knight SJ, Davies KE, Assman-Hulsmans CF, Oostra BA. Hamel BC, et al. Among authors: knight sj. Am J Hum Genet. 1994 Nov;55(5):923-31. Am J Hum Genet. 1994. PMID: 7977354 Free PMC article.

3

Molecular-cytogenetic detection of a deletion of 1p36.3.

Giraudeau F, Aubert D, Young I, Horsley S, Knight S, Kearney L, Vergnaud G, Flint J. Giraudeau F, et al. Among authors: knight s. J Med Genet. 1997 Apr;34(4):314-7. doi: 10.1136/jmg.34.4.314. J Med Genet. 1997. PMID: 9138156 Free PMC article.

4

Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres.

Knight SJ, Horsley SW, Regan R, Lawrie NM, Maher EJ, Cardy DL, Flint J, Kearney L. Knight SJ, et al. Eur J Hum Genet. 1997 Jan-Feb;5(1):1-8. Eur J Hum Genet. 1997. PMID: 9156314

5

Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome rearrangements.

Horsley SW, Knight SJ, Nixon J, Huson S, Fitchett M, Boone RA, Hilton-Jones D, Flint J, Kearney L. Horsley SW, et al. Among authors: knight sj. J Med Genet. 1998 Sep;35(9):722-6. doi: 10.1136/jmg.35.9.722. J Med Genet. 1998. PMID: 9733029 Free PMC article.

6

Screening for submicroscopic chromosome rearrangements in children with idiopathic mental retardation using microsatellite markers for the chromosome telomeres.

Slavotinek A, Rosenberg M, Knight S, Gaunt L, Fergusson W, Killoran C, Clayton-Smith J, Kingston H, Campbell RH, Flint J, Donnai D, Biesecker L. Slavotinek A, et al. Among authors: knight s. J Med Genet. 1999 May;36(5):405-11. J Med Genet. 1999. PMID: 10353788 Free PMC article.

7

A case of recurrent congenital fetal anomalies associated with a familial subtelomeric translocation.

Brackley KJ, Kilby MD, Morton J, Whittle MJ, Knight SJ, Flint J. Brackley KJ, et al. Among authors: knight sj. Prenat Diagn. 1999 Jun;19(6):570-4. Prenat Diagn. 1999. PMID: 10416976

8

Subtle chromosomal rearrangements in children with unexplained mental retardation.

Knight SJ, Regan R, Nicod A, Horsley SW, Kearney L, Homfray T, Winter RM, Bolton P, Flint J. Knight SJ, et al. Lancet. 1999 Nov 13;354(9191):1676-81. doi: 10.1016/S0140-6736(99)03070-6. Lancet. 1999. PMID: 10568569

9

Neurodevelopmental profile of a new dysmorphic syndrome associated with submicroscopic partial deletion of 1p36.3.

Knight-Jones E, Knight S, Heussler H, Regan R, Flint J, Martin K. Knight-Jones E, et al. Among authors: knight s. Dev Med Child Neurol. 2000 Mar;42(3):201-6. doi: 10.1017/s0012162200000347. Dev Med Child Neurol. 2000. PMID: 10755460 Free article.

10

Perfect endings: a review of subtelomeric probes and their use in clinical diagnosis.

Knight SJ, Flint J. Knight SJ, et al. J Med Genet. 2000 Jun;37(6):401-9. doi: 10.1136/jmg.37.6.401. J Med Genet. 2000. PMID: 10851249 Free PMC article. Review.

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