Webb T - Search Results

1

Further evidence for dominant inheritance at the chromosome 15q11-13 locus in familial Angelman syndrome.

Clayton-Smith J, Webb T, Robb SA, Dijkstra I, Willems P, Lam S, Cheng XJ, Pembrey ME, Malcolm S. Clayton-Smith J, et al. Among authors: webb t. Am J Med Genet. 1992 Sep 15;44(2):256-60. doi: 10.1002/ajmg.1320440236. Am J Med Genet. 1992. PMID: 1360768

2

Maternal origin of deletion 15q11-13 in 25/25 cases of Angelman syndrome.

Smith JC, Webb T, Pembrey ME, Nichols M, Malcolm S. Smith JC, et al. Among authors: webb t. Hum Genet. 1992 Feb;88(4):376-8. doi: 10.1007/BF00215668. Hum Genet. 1992. PMID: 1740313

3

Molecular mechanisms in Angelman syndrome: a survey of 93 patients.

Chan CT, Clayton-Smith J, Cheng XJ, Buxton J, Webb T, Pembrey ME, Malcolm S. Chan CT, et al. Among authors: webb t. J Med Genet. 1993 Nov;30(11):895-902. doi: 10.1136/jmg.30.11.895. J Med Genet. 1993. PMID: 7905534 Free PMC article.

4

Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome.

Clayton-Smith J, Driscoll DJ, Waters MF, Webb T, Andrews T, Malcolm S, Pembrey ME, Nicholls RD. Clayton-Smith J, et al. Among authors: webb t. Am J Med Genet. 1993 Oct 1;47(5):683-6. doi: 10.1002/ajmg.1320470519. Am J Med Genet. 1993. PMID: 8266996

5

Duplication of chromosome 15 in the region 15q11-13 in a patient with developmental delay and ataxia with similarities to Angelman syndrome.

Clayton-Smith J, Webb T, Cheng XJ, Pembrey ME, Malcolm S. Clayton-Smith J, et al. Among authors: webb t. J Med Genet. 1993 Jun;30(6):529-31. doi: 10.1136/jmg.30.6.529. J Med Genet. 1993. PMID: 8326502 Free PMC article. Review.

6

Inheritance of parental chromosomes 15 in Angelman syndrome--implications for the family.

Webb T, Malcolm S, Pembrey ME, Clayton-Smith J. Webb T, et al. Genet Couns. 1993;4(1):1-6. Genet Couns. 1993. PMID: 8471216

7

Angelman syndrome with a chromosomal inversion 15 inv(p11q13) accompanied by a deletion in 15q11q13.

Webb T, Clayton-Smith J, Cheng XJ, Knoll JH, Lalande M, Pembrey ME, Malcolm S. Webb T, et al. J Med Genet. 1992 Dec;29(12):921-4. doi: 10.1136/jmg.29.12.921. J Med Genet. 1992. PMID: 1362225 Free PMC article.

8

Uniparental paternal disomy in Angelman's syndrome.

Malcolm S, Clayton-Smith J, Nichols M, Robb S, Webb T, Armour JA, Jeffreys AJ, Pembrey ME. Malcolm S, et al. Among authors: webb t. Lancet. 1991 Mar 23;337(8743):694-7. doi: 10.1016/0140-6736(91)90278-w. Lancet. 1991. PMID: 1672177

9

Tightly linked polymorphic markers for fragile X syndrome and prenatal cytogenetic diagnostic experience.

Glass IA, Del Mastro RG, Lanyon WG, Raeburn JA, Kilpatrick MW, Webb TP, Connor JM. Glass IA, et al. Among authors: webb tp. Am J Med Genet. 1992 Aug 1;43(6):1050-6. doi: 10.1002/ajmg.1320430632. Am J Med Genet. 1992. PMID: 1415337

10

Delayed replication of Xq27 in individuals with the fragile X syndrome.

Webb T. Webb T. Am J Med Genet. 1992 Aug 1;43(6):1057-62. doi: 10.1002/ajmg.1320430633. Am J Med Genet. 1992. PMID: 1415338

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