Higgs DR - Search Results

1

Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome).

Gibbons RJ, Picketts DJ, Villard L, Higgs DR. Gibbons RJ, et al. Among authors: higgs dr. Cell. 1995 Mar 24;80(6):837-45. doi: 10.1016/0092-8674(95)90287-2. Cell. 1995. PMID: 7697714 Free 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

Cis-acting sequences regulating expression of the human alpha-globin cluster lie within constitutively open chromatin.

Vyas P, Vickers MA, Simmons DL, Ayyub H, Craddock CF, Higgs DR. Vyas P, et al. Among authors: higgs dr. Cell. 1992 May 29;69(5):781-93. doi: 10.1016/0092-8674(92)90290-s. Cell. 1992. PMID: 1591777

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: 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.

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. 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.

6

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.

7

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. Among authors: higgs dr. 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.

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. Among authors: higgs dr. 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. 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. 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.

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