Morrison N - Search Results

1

Chromosome 22q11 microdeletions in tetralogy of Fallot.

Trainer AH, Morrison N, Dunlop A, Wilson N, Tolmie J. Trainer AH, et al. Among authors: morrison n. Arch Dis Child. 1996 Jan;74(1):62-3. doi: 10.1136/adc.74.1.62. Arch Dis Child. 1996. PMID: 8660052 Free PMC article.

2

Towards earlier diagnosis of 22q11 deletions.

Tobias ES, Morrison N, Whiteford ML, Tolmie JL. Tobias ES, et al. Among authors: morrison n. Arch Dis Child. 1999 Dec;81(6):513-4. doi: 10.1136/adc.81.6.513. Arch Dis Child. 1999. PMID: 10569971 Free PMC article.

3

Clinical and molecular cytogenetic (FISH) diagnosis of Williams syndrome.

Brewer CM, Morrison N, Tolmie JL. Brewer CM, et al. Among authors: morrison n. Arch Dis Child. 1996 Jan;74(1):59-61. doi: 10.1136/adc.74.1.59. Arch Dis Child. 1996. PMID: 8660051 Free PMC article.

4

Chromosomal microarray analysis for looked after children: a double-edged sword?

Hamilton MJ, Tolmie JL, Joss S, Morrison N, Suhaimi NM. Hamilton MJ, et al. Among authors: morrison n. Arch Dis Child. 2015 Feb;100(2):206-7. doi: 10.1136/archdischild-2014-307189. Epub 2014 Sep 26. Arch Dis Child. 2015. PMID: 25260514 No abstract available.

5

Familial Wolf-Hirschhorn syndrome resulting from a cryptic translocation: a clinical and molecular study.

Reid E, Morrison N, Barron L, Boyd E, Cooke A, Fielding D, Tolmie JL. Reid E, et al. Among authors: morrison n. J Med Genet. 1996 Mar;33(3):197-202. doi: 10.1136/jmg.33.3.197. J Med Genet. 1996. PMID: 8728691 Free PMC article.

6

Familial Kleefstra syndrome due to maternal somatic mosaicism for interstitial 9q34.3 microdeletions.

Willemsen MH, Beunders G, Callaghan M, de Leeuw N, Nillesen WM, Yntema HG, van Hagen JM, Nieuwint AW, Morrison N, Keijzers-Vloet ST, Hoischen A, Brunner HG, Tolmie J, Kleefstra T. Willemsen MH, et al. Among authors: morrison n. Clin Genet. 2011 Jul;80(1):31-8. doi: 10.1111/j.1399-0004.2010.01607.x. Epub 2011 Jan 10. Clin Genet. 2011. PMID: 21204793

7

DNA copy number variations are important in the complex genetic architecture of müllerian disorders.

McGowan R, Tydeman G, Shapiro D, Craig T, Morrison N, Logan S, Balen AH, Ahmed SF, Deeny M, Tolmie J, Tobias ES. McGowan R, et al. Among authors: morrison n. Fertil Steril. 2015 Apr;103(4):1021-1030.e1. doi: 10.1016/j.fertnstert.2015.01.008. Epub 2015 Feb 20. Fertil Steril. 2015. PMID: 25707337 Free article.

8

17q21.31 microdeletion syndrome: further expanding the clinical phenotype.

Sharkey FH, Morrison N, Murray R, Iremonger J, Stephen J, Maher E, Tolmie J, Jackson AP. Sharkey FH, et al. Among authors: morrison n. Cytogenet Genome Res. 2009;127(1):61-6. doi: 10.1159/000279260. Epub 2010 Jan 27. Cytogenet Genome Res. 2009. PMID: 20110647

9

Absence of learning difficulties in a hyperactive boy with a terminal Xp deletion encompassing the MRX49 locus.

Tobias ES, Bryce G, Farmer G, Barton J, Colgan J, Morrison N, Cooke A, Tolmie JL. Tobias ES, et al. Among authors: morrison n. J Med Genet. 2001 Jul;38(7):466-70. doi: 10.1136/jmg.38.7.466. J Med Genet. 2001. PMID: 11474655 Free PMC article. No abstract available.

10

A practical strategy for detection of major chromosome aneuploidies using ratio-mixing fluorescence in situ hybridization.

Mohaddes SM, Boyd E, Morris A, Morrison N, Connor JM. Mohaddes SM, et al. Among authors: morrison n. Mol Cell Probes. 1996 Apr;10(2):147-54. doi: 10.1006/mcpr.1996.0020. Mol Cell Probes. 1996. PMID: 8737399

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