Laing N - Search Results

1

Refinement of the chromosome 5p locus for craniometaphyseal dysplasia.

Chandler D, Tinschert S, Lohan K, Harrop K, Goldblatt J, Nagy M, Hummel S, Braun HS, Laing N, Nürnberg P. Chandler D, et al. Among authors: laing n. Hum Genet. 2001 May;108(5):394-7. doi: 10.1007/s004390100515. Hum Genet. 2001. PMID: 11409866

2

Assignment of a gene (NEMI) for autosomal dominant nemaline myopathy to chromosome I.

Laing NG, Majda BT, Akkari PA, Layton MG, Mulley JC, Phillips H, Haan EA, White SJ, Beggs AH, Kunkel LM, et al. Laing NG, et al. Am J Hum Genet. 1992 Mar;50(3):576-83. Am J Hum Genet. 1992. PMID: 1347195 Free PMC article.

3

A TaqI map of the dystrophin gene useful for deletion and carrier status analysis.

Walker AP, Laing NG, Yamada T, Chandler DC, Kakulas BA, Bartlett RJ. Walker AP, et al. Among authors: laing ng. J Med Genet. 1992 Jan;29(1):14-9. doi: 10.1136/jmg.29.1.14. J Med Genet. 1992. PMID: 1552537 Free PMC article.

4

Two distinct mutations in a single dystrophin gene: chance occurrence or premutation?

Laing NG, Layton MG, Johnsen RD, Chandler DC, Mears ME, Goldblatt J, Kakulas BA. Laing NG, et al. Am J Med Genet. 1992 Mar 1;42(5):688-92. doi: 10.1002/ajmg.1320420512. Am J Med Genet. 1992. PMID: 1632439

5

The diagnosis of Duchenne and Becker muscular dystrophies: two years' experience in a comprehensive carrier screening and prenatal diagnostic laboratory.

Laing NG, Mears ME, Chandler DC, Layton MG, Thomas HE, Johnsen RD, Goldblatt J, Kakulas BA. Laing NG, et al. Med J Aust. 1991 Jan 7;154(1):14-8. doi: 10.5694/j.1326-5377.1991.tb112839.x. Med J Aust. 1991. PMID: 1670611

6

Identification of Duchenne muscular dystrophy genomic probe P20 constant Taql fragment corresponding to the EcoRV and Mspl polymorphisms.

Laing NG, Walker AP, Akkari PA, Chandler DC, Layton MG, Mears ME, Yamada T, Bartlett RJ, Pericak-Vance MA, Hung WY, et al. Laing NG, et al. Prenat Diagn. 1991 Jan;11(1):63-7. doi: 10.1002/pd.1970110112. Prenat Diagn. 1991. PMID: 1709287

7

Duchenne muscular dystrophy (DMD) gene cDNA 8 PstI and TaqI polymorphisms involve exon 51 of the HindIII map.

Laing NG, Akkari PA, Chandler DC, Thomas HE, Layton MG, Mears ME, Kakulas BA. Laing NG, et al. Nucleic Acids Res. 1990 Jul 25;18(14):4284. doi: 10.1093/nar/18.14.4284. Nucleic Acids Res. 1990. PMID: 1974044 Free PMC article. No abstract available.

8

Differentiation of Becker muscular dystrophy from limb-girdle muscular dystrophy and Kugelberg-Welander disease using a cDNA probe.

Laing NG, Mears ME, Thomas HE, Chandler DC, Layton MG, Goldblatt J, Kakulas BA. Laing NG, et al. Med J Aust. 1990 Mar 5;152(5):270-1. doi: 10.5694/j.1326-5377.1990.tb120926.x. Med J Aust. 1990. PMID: 2255288

9

A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy.

Laing NG, Wilton SD, Akkari PA, Dorosz S, Boundy K, Kneebone C, Blumbergs P, White S, Watkins H, Love DR, et al. Laing NG, et al. Nat Genet. 1995 Jan;9(1):75-9. doi: 10.1038/ng0195-75. Nat Genet. 1995. PMID: 7704029

10

Autosomal dominant distal myopathy: linkage to chromosome 14.

Laing NG, Laing BA, Meredith C, Wilton SD, Robbins P, Honeyman K, Dorosz S, Kozman H, Mastaglia FL, Kakulas BA. Laing NG, et al. Among authors: laing ba. Am J Hum Genet. 1995 Feb;56(2):422-7. Am J Hum Genet. 1995. PMID: 7847377 Free PMC article.

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