Higgs DR - Search Results

1

Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes.

McDowell TL, Gibbons RJ, Sutherland H, O'Rourke DM, Bickmore WA, Pombo A, Turley H, Gatter K, Picketts DJ, Buckle VJ, Chapman L, Rhodes D, Higgs DR. McDowell TL, et al. Among authors: higgs dr. Proc Natl Acad Sci U S A. 1999 Nov 23;96(24):13983-8. doi: 10.1073/pnas.96.24.13983. Proc Natl Acad Sci U S A. 1999. PMID: 10570185 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: higgs dr. Am J Hum Genet. 1992 Nov;51(5):1136-49. Am J Hum Genet. 1992. PMID: 1415255 Free PMC article.

3

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: higgs dr. 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.

4

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. Among authors: higgs dr. 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.

5

The non-deletion alpha thalassaemia/mental retardation syndrome: further support for X linkage.

Donnai D, Clayton-Smith J, Gibbons RJ, Higgs DR. Donnai D, et al. Among authors: higgs dr. J Med Genet. 1991 Nov;28(11):742-5. doi: 10.1136/jmg.28.11.742. J Med Genet. 1991. PMID: 1770530 Free PMC article.

6

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. Among authors: higgs dr. Cell. 1991 Feb 8;64(3):595-606. doi: 10.1016/0092-8674(91)90243-r. Cell. 1991. PMID: 1991321

7

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. Among authors: higgs dr. Am J Hum Genet. 1990 Jun;46(6):1127-40. Am J Hum Genet. 1990. PMID: 2339705 Free PMC article.

8

Alpha-thalassemia caused by a large (62 kb) deletion upstream of the human alpha globin gene cluster.

Hatton CS, Wilkie AO, Drysdale HC, Wood WG, Vickers MA, Sharpe J, Ayyub H, Pretorius IM, Buckle VJ, Higgs DR. Hatton CS, et al. Among authors: higgs dr. Blood. 1990 Jul 1;76(1):221-7. Blood. 1990. PMID: 2364173 Free article.

9

Detection of breakpoints in submicroscopic chromosomal translocation, illustrating an important mechanism for genetic disease.

Lamb J, Wilkie AO, Harris PC, Buckle VJ, Lindenbaum RH, Barton NJ, Reeders ST, Weatherall DJ, Higgs DR. Lamb J, et al. Among authors: higgs dr. Lancet. 1989 Oct 7;2(8667):819-24. doi: 10.1016/s0140-6736(89)92995-4. Lancet. 1989. PMID: 2477654

10

Localisation of human alpha globin to 16p13.3----pter.

Buckle VJ, Higgs DR, Wilkie AO, Super M, Weatherall DJ. Buckle VJ, et al. Among authors: higgs dr. J Med Genet. 1988 Dec;25(12):847-9. doi: 10.1136/jmg.25.12.847. J Med Genet. 1988. PMID: 3236367 Free PMC article.

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