Nouri S - Search Results

1

High-throughput analysis of chromosome abnormality in spontaneous miscarriage using an MLPA subtelomere assay with an ancillary FISH test for polyploidy.

Bruno DL, Burgess T, Ren H, Nouri S, Pertile MD, Francis DI, Norris F, Kenney BK, Schouten J, Andy Choo KH, Slater HR. Bruno DL, et al. Among authors: nouri s. Am J Med Genet A. 2006 Dec 15;140(24):2786-93. doi: 10.1002/ajmg.a.31552. Am J Med Genet A. 2006. PMID: 17106871

2

Improved testing for CMT1A and HNPP using multiplex ligation-dependent probe amplification (MLPA) with rapid DNA preparations: comparison with the interphase FISH method.

Slater H, Bruno D, Ren H, La P, Burgess T, Hills L, Nouri S, Schouten J, Choo KH. Slater H, et al. Among authors: nouri s. Hum Mutat. 2004 Aug;24(2):164-71. doi: 10.1002/humu.20072. Hum Mutat. 2004. PMID: 15241798

3

Unstable Robertsonian translocations der(13;15)(q10;q10): heritable chromosome fission without phenotypic effect in two kindreds.

Perry J, White SM, Nouri S, Bain SM, Hutchinson RG, La P, Northrop E, Eyre HJ, Pertile MD, Hocking TA, Thompson EM, Yu S, Choo KH, Slater HR. Perry J, et al. Among authors: nouri s. Am J Med Genet A. 2005 Jul 1;136(1):25-30. doi: 10.1002/ajmg.a.30763. Am J Med Genet A. 2005. PMID: 15889410

4

Pericentromeric euchromatin is conserved in minute human supernumerary chromosomes: a study using cross-species colour segmenting (RxFISH).

Hills LV, Nouri S, Slater HR. Hills LV, et al. Among authors: nouri s. Chromosome Res. 2003;11(4):359-63. doi: 10.1023/a:1024096024847. Chromosome Res. 2003. PMID: 12906132

5

Molecular distinction between true centric fission and pericentric duplication-fission.

Perry J, Nouri S, La P, Daniel A, Wu Z, Purvis-Smith S, Northrop E, Choo KH, Slater HR. Perry J, et al. Among authors: nouri s. Hum Genet. 2005 Mar;116(4):300-10. doi: 10.1007/s00439-004-1209-4. Epub 2005 Jan 27. Hum Genet. 2005. PMID: 15712016

6

Monosomy 21 seen in live born is unlikely to represent true monosomy 21: a case report and review of the literature.

Burgess T, Downie L, Pertile MD, Francis D, Glass M, Nouri S, Pszczola R. Burgess T, et al. Among authors: nouri s. Case Rep Genet. 2014;2014:965401. doi: 10.1155/2014/965401. Epub 2014 Feb 4. Case Rep Genet. 2014. PMID: 24649383 Free PMC article.

7

Neocentromere formation in a stable ring 1p32-p36.1 chromosome.

Slater HR, Nouri S, Earle E, Lo AW, Hale LG, Choo KH. Slater HR, et al. Among authors: nouri s. J Med Genet. 1999 Dec;36(12):914-8. J Med Genet. 1999. PMID: 10593999 Free PMC article.

8

Increased gene dosage at Xq26-q27 is associated with X-linked hypopituitarism.

Solomon NM, Nouri S, Warne GL, Lagerström-Fermér M, Forrest SM, Thomas PQ. Solomon NM, et al. Among authors: nouri s. Genomics. 2002 Apr;79(4):553-9. doi: 10.1006/geno.2002.6741. Genomics. 2002. PMID: 11944988

9

Fetal nucleated red blood cells from CVS washings: an aid to development of first trimester non-invasive prenatal diagnosis.

Voullaire L, Ioannou P, Nouri S, Williamson R. Voullaire L, et al. Among authors: nouri s. Prenat Diagn. 2001 Oct;21(10):827-34. Prenat Diagn. 2001. PMID: 11746123

10

Novel endogenous type D retroviral particles expressed at high levels in a SCID mouse thymic lymphoma.

Ristevski S, Purcell DF, Marshall J, Campagna D, Nouri S, Fenton SP, McPhee DA, Kannourakis G. Ristevski S, et al. Among authors: nouri s. J Virol. 1999 Jun;73(6):4662-9. doi: 10.1128/JVI.73.6.4662-4669.1999. J Virol. 1999. PMID: 10233925 Free PMC article.

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