Wilkie AO - Search Results

1

Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. II. Cases without detectable abnormality of the alpha globin complex.

Wilkie AO, Zeitlin HC, Lindenbaum RH, Buckle VJ, Fischel-Ghodsian N, Chui DH, Gardner-Medwin D, MacGillivray MH, Weatherall DJ, Higgs DR. Wilkie AO, et al. Am J Hum Genet. 1990 Jun;46(6):1127-40. Am J Hum Genet. 1990. PMID: 2339705 Free PMC article.

2

X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome: localization to Xq12-q21.31 by X inactivation and linkage analysis.

Gibbons RJ, Suthers GK, Wilkie AO, Buckle VJ, Higgs DR. Gibbons RJ, et al. Among authors: wilkie ao. Am J Hum Genet. 1992 Nov;51(5):1136-49. Am J Hum Genet. 1992. PMID: 1415255 Free PMC article.

3

An unusually large (CA)n repeat in the region of divergence between subtelomeric alleles of human chromosome 16p.

Wilkie AO, Higgs DR. Wilkie AO, et al. Genomics. 1992 May;13(1):81-8. doi: 10.1016/0888-7543(92)90205-7. Genomics. 1992. PMID: 1577495

4

A newly defined X linked mental retardation syndrome associated with alpha thalassaemia.

Gibbons RJ, Wilkie AO, Weatherall DJ, Higgs DR. Gibbons RJ, et al. Among authors: wilkie ao. J Med Genet. 1991 Nov;28(11):729-33. doi: 10.1136/jmg.28.11.729. J Med Genet. 1991. PMID: 1770527 Free PMC article. Review. No abstract available.

5

X linked alpha thalassaemia/mental retardation: spectrum of clinical features in three related males.

Wilkie AO, Gibbons RJ, Higgs DR, Pembrey ME. Wilkie AO, et al. J Med Genet. 1991 Nov;28(11):738-41. doi: 10.1136/jmg.28.11.738. J Med Genet. 1991. PMID: 1770529 Free PMC article.

6

The non-deletion type of alpha thalassaemia/mental retardation: a recognisable dysmorphic syndrome with X linked inheritance.

Wilkie AO, Pembrey ME, Gibbons RJ, Higgs DR, Porteous ME, Burn J, Winter RM. Wilkie AO, et al. J Med Genet. 1991 Oct;28(10):724. doi: 10.1136/jmg.28.10.724. J Med Genet. 1991. PMID: 1941971 Free PMC article. No abstract available.

7

A truncated human chromosome 16 associated with alpha thalassaemia is stabilized by addition of telomeric repeat (TTAGGG)n.

Wilkie AO, Lamb J, Harris PC, Finney RD, Higgs DR. Wilkie AO, et al. Nature. 1990 Aug 30;346(6287):868-71. doi: 10.1038/346868a0. Nature. 1990. PMID: 1975428

8

Stable length polymorphism of up to 260 kb at the tip of the short arm of human chromosome 16.

Wilkie AO, Higgs DR, Rack KA, Buckle VJ, Spurr NK, Fischel-Ghodsian N, Ceccherini I, Brown WR, Harris PC. Wilkie AO, et al. Cell. 1991 Feb 8;64(3):595-606. doi: 10.1016/0092-8674(91)90243-r. Cell. 1991. PMID: 1991321

9

The alpha-thalassemias.

Higgs DR, Wood WG, Jarman AP, Vickers MA, Wilkie AO, Lamb J, Vyas P, Bennett JP. Higgs DR, et al. Among authors: wilkie ao. Ann N Y Acad Sci. 1990;612:15-22. doi: 10.1111/j.1749-6632.1990.tb24286.x. Ann N Y Acad Sci. 1990. PMID: 2291543 Review. No abstract available.

10

Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3.

Wilkie AO, Buckle VJ, Harris PC, Lamb J, Barton NJ, Reeders ST, Lindenbaum RH, Nicholls RD, Barrow M, Bethlenfalvay NC, et al. Wilkie AO, et al. Am J Hum Genet. 1990 Jun;46(6):1112-26. Am J Hum Genet. 1990. PMID: 2339704 Free PMC article.

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