Laing NG - Search Results

1

Correspondence on "Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG)" by Gregg et al.

Righetti S, Dive L, Archibald AD, Freeman L, McClaren B, Kanga-Parabia A, Delatycki MB, Laing NG, Kirk EP, Newson AJ; counselling, psycho-social, and implementation science teams at Mackenzie’s Mission and the Gene Selection Committee. Righetti S, et al. Among authors: laing ng. Genet Med. 2022 May;24(5):1158-1161. doi: 10.1016/j.gim.2022.01.007. Epub 2022 Feb 12. Genet Med. 2022. PMID: 35168887 Free article. No abstract available.

2

Effects of MECP2 mutation type, location and X-inactivation in modulating Rett syndrome phenotype.

Weaving LS, Williamson SL, Bennetts B, Davis M, Ellaway CJ, Leonard H, Thong MK, Delatycki M, Thompson EM, Laing N, Christodoulou J. Weaving LS, et al. Am J Med Genet A. 2003 Apr 15;118A(2):103-14. doi: 10.1002/ajmg.a.10053. Am J Med Genet A. 2003. PMID: 12655490

3

Two major histocompatibility complex haplotypes influence susceptibility to sporadic inclusion body myositis: critical evaluation of an association with HLA-DR3.

Price P, Santoso L, Mastaglia F, Garlepp M, Kok CC, Allcock R, Laing N. Price P, et al. Tissue Antigens. 2004 Nov;64(5):575-80. doi: 10.1111/j.1399-0039.2004.00310.x. Tissue Antigens. 2004. PMID: 15496200

4

Sporadic inclusion body myositis in Japanese is associated with the MHC ancestral haplotype 52.1.

Scott AP, Allcock RJ, Mastaglia F, Nishino I, Nonaka I, Laing N. Scott AP, et al. Neuromuscul Disord. 2006 May;16(5):311-5. doi: 10.1016/j.nmd.2006.02.002. Epub 2006 Mar 24. Neuromuscul Disord. 2006. PMID: 16564169

5

Clinical utility gene card for: Laing distal myopathy.

Lamont P, Wallefeld W, Davis M, Udd B, Laing N. Lamont P, et al. Eur J Hum Genet. 2011 Mar;19(3). doi: 10.1038/ejhg.2010.190. Epub 2010 Dec 8. Eur J Hum Genet. 2011. PMID: 21150886 Free PMC article. No abstract available.

6

Recombination mapping of the susceptibility region for sporadic inclusion body myositis within the major histocompatibility complex.

Scott AP, Laing NG, Mastaglia F, Needham M, Walter MC, Dalakas MC, Allcock RJ. Scott AP, et al. Among authors: laing ng. J Neuroimmunol. 2011 Jun;235(1-2):77-83. doi: 10.1016/j.jneuroim.2011.02.011. Epub 2011 May 2. J Neuroimmunol. 2011. PMID: 21543121

7

Molecular diagnosis of duchenne muscular dystrophy: past, present and future in relation to implementing therapies.

Laing NG, Davis MR, Bayley K, Fletcher S, Wilton SD. Laing NG, et al. Clin Biochem Rev. 2011 Aug;32(3):129-34. Clin Biochem Rev. 2011. PMID: 21912442 Free PMC article.

8

Clinical utility gene card for: nemaline myopathy.

Nowak KJ, Davis MR, Wallgren-Pettersson C, Lamont PJ, Laing NG. Nowak KJ, et al. Among authors: laing ng. Eur J Hum Genet. 2012 Jun;20(6). doi: 10.1038/ejhg.2012.70. Epub 2012 Apr 18. Eur J Hum Genet. 2012. PMID: 22510848 Free PMC article. No abstract available.

9

Investigation of NOTCH4 coding region polymorphisms in sporadic inclusion body myositis.

Scott AP, Laing NG, Mastaglia F, Dalakas M, Needham M, Allcock RJ. Scott AP, et al. Among authors: laing ng. J Neuroimmunol. 2012 Sep 15;250(1-2):66-70. doi: 10.1016/j.jneuroim.2012.04.021. Epub 2012 Jun 23. J Neuroimmunol. 2012. PMID: 22732452

10

Whole exome sequencing in foetal akinesia expands the genotype-phenotype spectrum of GBE1 glycogen storage disease mutations.

Ravenscroft G, Thompson EM, Todd EJ, Yau KS, Kresoje N, Sivadorai P, Friend K, Riley K, Manton ND, Blumbergs P, Fietz M, Duff RM, Davis MR, Allcock RJ, Laing NG. Ravenscroft G, et al. Among authors: laing ng. Neuromuscul Disord. 2013 Feb;23(2):165-9. doi: 10.1016/j.nmd.2012.11.005. Epub 2012 Dec 3. Neuromuscul Disord. 2013. PMID: 23218673

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