Lomax B - Search Results

1

A 5-Mb microdeletion at 6q16.1-q16.3 with SIM gene deletion and obesity.

Wang JC, Turner L, Lomax B, Eydoux P. Wang JC, et al. Among authors: lomax b. Am J Med Genet A. 2008 Nov 15;146A(22):2975-8. doi: 10.1002/ajmg.a.32555. Am J Med Genet A. 2008. PMID: 18925680 No abstract available.

2

Craniosynostosis associated with distal 5q-trisomy: further evidence that extra copy of MSX2 gene leads to craniosynostosis.

Wang JC, Steinraths M, Dang L, Lomax B, Eydoux P, Stockley T, Yong SL, Van Allen MI. Wang JC, et al. Among authors: lomax b. Am J Med Genet A. 2007 Dec 15;143A(24):2931-6. doi: 10.1002/ajmg.a.31946. Am J Med Genet A. 2007. PMID: 17955513

3

Inverted duplication with terminal deletion of 5p and no cat-like cry.

Wang JC, Coe BP, Lomax B, MacLeod PM, Parslow MI, Schein JE, Lam WL, Eydoux P. Wang JC, et al. Among authors: lomax b. Am J Med Genet A. 2008 May 1;146A(9):1173-9. doi: 10.1002/ajmg.a.32246. Am J Med Genet A. 2008. PMID: 18266247

4

Molecular breakpoint mapping of 6q11-q14 interstitial deletions in seven patients.

Wang JC, Dang L, Lomax B, Turner L, Shago M, Teebi AS, Klatt R, MacLeod PM, Yong SL, Nowaczyk MJ, Eydoux P. Wang JC, et al. Among authors: lomax b. Am J Med Genet A. 2009 Mar;149A(3):372-9. doi: 10.1002/ajmg.a.32675. Am J Med Genet A. 2009. PMID: 19213033

5

BPES with atypical premature ovarian insufficiency, and evidence of mitotic recombination, in a woman with trisomy X and a translocation t(3;11)(q22.3;q14.1).

Schlade-Bartusiak K, Brown L, Lomax B, Bruyère H, Gillan T, Hamilton S, McGillivray B, Eydoux P. Schlade-Bartusiak K, et al. Among authors: lomax b. Am J Med Genet A. 2012 Sep;158A(9):2322-7. doi: 10.1002/ajmg.a.35516. Epub 2012 Aug 6. Am J Med Genet A. 2012. PMID: 22887799

6

A hemizygous SCO2 mutation in an early onset rapidly progressive, fatal cardiomyopathy.

Leary SC, Mattman A, Wai T, Koehn DC, Clarke LA, Chan S, Lomax B, Eydoux P, Vallance HD, Shoubridge EA. Leary SC, et al. Among authors: lomax b. Mol Genet Metab. 2006 Sep-Oct;89(1-2):129-33. doi: 10.1016/j.ymgme.2006.04.016. Epub 2006 Jun 9. Mol Genet Metab. 2006. PMID: 16765077

7

Comparative genomic hybridization: a new approach to screening for intrauterine complete or mosaic aneuploidy.

Lestou VS, Desilets V, Lomax BL, Barrett IJ, Wilson RD, Langlois S, Kalousek DK. Lestou VS, et al. Among authors: lomax bl. Am J Med Genet. 2000 Jun 5;92(4):281-4. doi: 10.1002/(sici)1096-8628(20000605)92:4<281::aid-ajmg12>3.0.co;2-s. Am J Med Genet. 2000. PMID: 10842297

8

Detection of confined placental mosaicism in trisomy 18 conceptions using interphase cytogenetic analysis.

Harrison KJ, Barrett IJ, Lomax BL, Kuchinka BD, Kalousek DK. Harrison KJ, et al. Among authors: lomax bl. Hum Genet. 1993 Oct;92(4):353-8. doi: 10.1007/BF01247334. Hum Genet. 1993. PMID: 8225315

9

Comparative genomic hybridization in combination with flow cytometry improves results of cytogenetic analysis of spontaneous abortions.

Lomax B, Tang S, Separovic E, Phillips D, Hillard E, Thomson T, Kalousek DK. Lomax B, et al. Am J Hum Genet. 2000 May;66(5):1516-21. doi: 10.1086/302878. Epub 2000 Mar 30. Am J Hum Genet. 2000. PMID: 10741955 Free PMC article.

10

Interphase cytogenetic analysis of single cell suspensions prepared from previously formalin-fixed and paraffin-embedded tissues.

Kuchinka BD, Kalousek DK, Lomax BL, Harrison KJ, Barrett IJ. Kuchinka BD, et al. Among authors: lomax bl. Mod Pathol. 1995 Feb;8(2):183-6. Mod Pathol. 1995. PMID: 7777481

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