Thomas NS - Search Results

1

Intragenic deletions in 164 boys with Duchenne muscular dystrophy (DMD) studied with dystrophin cDNA.

Upadhyaya M, Smith RA, Thomas NS, Norman AM, Harper PS. Upadhyaya M, et al. Among authors: thomas ns. Clin Genet. 1990 Jun;37(6):456-62. doi: 10.1111/j.1399-0004.1990.tb03530.x. Clin Genet. 1990. PMID: 2200624

2

Distinction of Becker from limb-girdle muscular dystrophy by means of dystrophin cDNA probes.

Norman A, Thomas N, Coakley J, Harper P. Norman A, et al. Lancet. 1989 Mar 4;1(8636):466-8. doi: 10.1016/s0140-6736(89)91367-6. Lancet. 1989. PMID: 2563842

3

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

4

Becker muscular dystrophy: correlation of deletion type with clinical severity.

Norman AM, Thomas NS, Kingston HM, Harper PS. Norman AM, et al. Among authors: thomas ns. J Med Genet. 1990 Apr;27(4):236-9. doi: 10.1136/jmg.27.4.236. J Med Genet. 1990. PMID: 2325103 Free PMC article.

5

Duchenne muscular dystrophy in Wales: impact of DNA linkage analysis and cDNA deletion screening.

Norman AM, Upadhyaya M, Thomas NS, Roberts K, Harper PS. Norman AM, et al. Among authors: thomas ns. J Med Genet. 1989 Sep;26(9):565-71. doi: 10.1136/jmg.26.9.565. J Med Genet. 1989. PMID: 2810340 Free PMC article.

6

Molecular deletion analysis in Duchenne muscular dystrophy.

Thomas NS, Ray PN, Worton RG, Harper PS. Thomas NS, et al. J Med Genet. 1986 Dec;23(6):509-15. doi: 10.1136/jmg.23.6.509. J Med Genet. 1986. PMID: 2879923 Free PMC article.

7

Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy.

Malhotra SB, Hart KA, Klamut HJ, Thomas NS, Bodrug SE, Burghes AH, Bobrow M, Harper PS, Thompson MW, Ray PN, et al. Malhotra SB, et al. Among authors: thomas ns. Science. 1988 Nov 4;242(4879):755-9. doi: 10.1126/science.3055295. Science. 1988. PMID: 3055295

8

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.

9

Prenatal diagnosis of Duchenne dystrophy.

Harper PS, Williams H, Thomas N, Sarfarazi M. Harper PS, et al. Lancet. 1985 Apr 13;1(8433):872. doi: 10.1016/s0140-6736(85)92229-9. Lancet. 1985. PMID: 2858728 No abstract available.

10

The use of flanking markers in prediction for Duchenne muscular dystrophy.

Williams H, Sarfarazi M, Brown C, Thomas N, Harper PS. Williams H, et al. Arch Dis Child. 1986 Mar;61(3):218-22. doi: 10.1136/adc.61.3.218. Arch Dis Child. 1986. PMID: 3457554 Free PMC article.

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