Thomas NS - Search Results

1

Maternal folate polymorphisms and the etiology of human nondisjunction.

Hassold TJ, Burrage LC, Chan ER, Judis LM, Schwartz S, James SJ, Jacobs PA, Thomas NS. Hassold TJ, et al. Among authors: thomas ns. Am J Hum Genet. 2001 Aug;69(2):434-9. doi: 10.1086/321971. Epub 2001 Jul 5. Am J Hum Genet. 2001. PMID: 11443546 Free PMC article.

2

Maternal sex chromosome non-disjunction: evidence for X chromosome-specific risk factors.

Thomas NS, Ennis S, Sharp AJ, Durkie M, Hassold TJ, Collins AR, Jacobs PA. Thomas NS, et al. Hum Mol Genet. 2001 Feb 1;10(3):243-50. doi: 10.1093/hmg/10.3.243. Hum Mol Genet. 2001. PMID: 11159943

3

Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunction.

Borel C, Cheung F, Stewart H, Koolen DA, Phillips C, Thomas NS, Jacobs PA, Eliez S, Sharp AJ. Borel C, et al. Among authors: thomas ns. Hum Genet. 2012 Sep;131(9):1519-24. doi: 10.1007/s00439-012-1180-4. Epub 2012 May 30. Hum Genet. 2012. PMID: 22643917

4

A reinvestigation of non-disjunction resulting in 47, XXY males of paternal origin.

Thomas NS, Collins AR, Hassold TJ, Jacobs PA. Thomas NS, et al. Eur J Hum Genet. 2000 Oct;8(10):805-8. doi: 10.1038/sj.ejhg.5200531. Eur J Hum Genet. 2000. PMID: 11039584

5

Aberrant recombination and the origin of Klinefelter syndrome.

Thomas NS, Hassold TJ. Thomas NS, et al. Hum Reprod Update. 2003 Jul-Aug;9(4):309-17. doi: 10.1093/humupd/dmg028. Hum Reprod Update. 2003. PMID: 12926525 Review.

6

Functional disomy resulting from duplications of distal Xq in four unrelated patients.

Lachlan KL, Collinson MN, Sandford RO, van Zyl B, Jacobs PA, Thomas NS. Lachlan KL, et al. Among authors: thomas ns. Hum Genet. 2004 Oct;115(5):399-408. doi: 10.1007/s00439-004-1175-x. Epub 2004 Aug 24. Hum Genet. 2004. PMID: 15338277

7

Investigation of the origins of human autosomal inversions.

Thomas NS, Bryant V, Maloney V, Cockwell AE, Jacobs PA. Thomas NS, et al. Hum Genet. 2008 Jul;123(6):607-16. doi: 10.1007/s00439-008-0510-z. Epub 2008 May 10. Hum Genet. 2008. PMID: 18470537

8

A study of females with deletions of the short arm of the X chromosome.

James RS, Coppin B, Dalton P, Dennis NR, Mitchell C, Sharp AJ, Skuse DH, Thomas NS, Jacobs PA. James RS, et al. Among authors: thomas ns. Hum Genet. 1998 May;102(5):507-16. doi: 10.1007/s004390050733. Hum Genet. 1998. PMID: 9654198

9

Molecular and fluorescence in situ hybridization characterization of the breakpoints in 46 large supernumerary marker 15 chromosomes reveals an unexpected level of complexity.

Roberts SE, Maggouta F, Thomas NS, Jacobs PA, Crolla JA. Roberts SE, et al. Among authors: thomas ns. Am J Hum Genet. 2003 Nov;73(5):1061-72. doi: 10.1086/379155. Epub 2003 Oct 14. Am J Hum Genet. 2003. PMID: 14560400 Free PMC article.

10

A clinical and molecular study of 26 females with Xp deletions with special emphasis on inherited deletions.

Lachlan KL, Youings S, Costa T, Jacobs PA, Thomas NS. Lachlan KL, et al. Among authors: thomas ns. Hum Genet. 2006 Jan;118(5):640-51. doi: 10.1007/s00439-005-0081-1. Epub 2005 Nov 8. Hum Genet. 2006. PMID: 16283387

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