Thomas NS - Search Results

1

Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindred.

Wright AF, Bhattacharya SS, Aldred MA, Jay M, Carothers AD, Thomas NS, Bird AC, Jay B, Evans HJ. Wright AF, et al. Among authors: thomas ns. J Med Genet. 1991 Jul;28(7):453-7. doi: 10.1136/jmg.28.7.453. J Med Genet. 1991. PMID: 1895315 Free PMC article.

2

Molecular analysis of 20 patients with 2q37.3 monosomy: definition of minimum deletion intervals for key phenotypes.

Aldred MA, Sanford RO, Thomas NS, Barrow MA, Wilson LC, Brueton LA, Bonaglia MC, Hennekam RC, Eng C, Dennis NR, Trembath RC. Aldred MA, et al. Among authors: thomas ns. J Med Genet. 2004 Jun;41(6):433-9. doi: 10.1136/jmg.2003.017202. J Med Genet. 2004. PMID: 15173228 Free PMC article. No abstract available.

3

Detection of de novo mutations and analysis of their origin in families with X linked hypohidrotic ectodermal dysplasia.

Zonana J, Jones M, Clarke A, Gault J, Muller B, Thomas NS. Zonana J, et al. Among authors: thomas ns. J Med Genet. 1994 Apr;31(4):287-92. doi: 10.1136/jmg.31.4.287. J Med Genet. 1994. PMID: 8071953 Free PMC article.

4

X linked neonatal centronuclear/myotubular myopathy: evidence for linkage to Xq28 DNA marker loci.

Thomas NS, Williams H, Cole G, Roberts K, Clarke A, Liechti-Gallati S, Braga S, Gerber A, Meier C, Moser H, et al. Thomas NS, et al. J Med Genet. 1990 May;27(5):284-7. doi: 10.1136/jmg.27.5.284. J Med Genet. 1990. PMID: 2352256 Free PMC article.

5

Prenatal diagnosis of X-linked hypohidrotic ectodermal dysplasia by linkage analysis.

Zonana J, Schinzel A, Upadhyaya M, Thomas NS, Anton-Lamprecht I, Harper PS. Zonana J, et al. Among authors: thomas ns. Am J Med Genet. 1990 Jan;35(1):132-5. doi: 10.1002/ajmg.1320350125. Am J Med Genet. 1990. PMID: 2301463

6

Localisation of the gene for Emery-Dreifuss muscular dystrophy to the distal long arm of the X chromosome.

Thomas NS, Williams H, Elsas LJ, Hopkins LC, Sarfarazi M, Harper PS. Thomas NS, et al. J Med Genet. 1986 Dec;23(6):596-8. doi: 10.1136/jmg.23.6.596. J Med Genet. 1986. PMID: 3100805 Free PMC article.

7

X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis.

Zonana J, Clarke A, Sarfarazi M, Thomas NS, Roberts K, Marymee K, Harper PS. Zonana J, et al. Among authors: thomas ns. Am J Hum Genet. 1988 Jul;43(1):75-85. Am J Hum Genet. 1988. PMID: 3163892 Free PMC article.

8

X chromosome linkage studies in familial Rett syndrome.

Curtis AR, Headland S, Lindsay S, Thomas NS, Boye E, Kamakari S, Roustan P, Anvret M, Wahlstrom J, McCarthy G, et al. Curtis AR, et al. Among authors: thomas ns. Hum Genet. 1993 Jan;90(5):551-5. doi: 10.1007/BF00217457. Hum Genet. 1993. PMID: 8094068

9

Physical fine mapping of genes underlying X-linked deafness and non fra (X)-X-linked mental retardation at Xq21.

Bach I, Robinson D, Thomas N, Ropers HH, Cremers FP. Bach I, et al. Hum Genet. 1992 Aug;89(6):620-4. doi: 10.1007/BF00221950. Hum Genet. 1992. PMID: 1511979

10

Genetic heterogeneity in X-linked amelogenesis imperfecta.

Aldred MJ, Crawford PJ, Roberts E, Gillespie CM, Thomas NS, Fenton I, Sandkuijl LA, Harper PS. Aldred MJ, et al. Among authors: thomas ns. Genomics. 1992 Nov;14(3):567-73. doi: 10.1016/s0888-7543(05)80153-3. Genomics. 1992. PMID: 1358807

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