Bingham EA - Search Results

1

A missense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia in a family of Irish travellers.

Ahmad W, Irvine AD, Lam H, Buckley C, Bingham EA, Panteleyev AA, Ahmad M, McGrath JA, Christiano AM. Ahmad W, et al. Among authors: bingham ea. Am J Hum Genet. 1998 Oct;63(4):984-91. doi: 10.1086/302069. Am J Hum Genet. 1998. PMID: 9758627 Free PMC article.

2

A mutation detection strategy for the human keratin 6A gene and novel missense mutations in two cases of pachyonychia congenita type 1.

Smith FJ, McKenna KE, Irvine AD, Bingham EA, Coleman CM, Uitto J, McLean WH. Smith FJ, et al. Among authors: bingham ea. Exp Dermatol. 1999 Apr;8(2):109-14. doi: 10.1111/j.1600-0625.1999.tb00356.x. Exp Dermatol. 1999. PMID: 10232400

3

Focal dermal hypoplasia (Goltz syndrome) associated with intestinal malrotation and mediastinal dextroposition.

Irvine AD, Stewart FJ, Bingham EA, Nevin NC, Boston VE. Irvine AD, et al. Among authors: bingham ea. Am J Med Genet. 1996 Mar 29;62(3):213-5. doi: 10.1002/(SICI)1096-8628(19960329)62:3<213::AID-AJMG2>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8882775

4

An autosomal dominant syndrome of acromegaloid facial appearance and generalised hypertrichosis terminalis.

Irvine AD, Dolan OM, Hadden DR, Stewart FJ, Bingham EA, Nevin NC. Irvine AD, et al. Among authors: bingham ea. J Med Genet. 1996 Nov;33(11):972-4. doi: 10.1136/jmg.33.11.972. J Med Genet. 1996. PMID: 8950682 Free PMC article.

5

Microscopic polyangiitis. Delineation of a cutaneous-limited variant associated with antimyeloperoxidase autoantibody.

Irvine AD, Bruce IN, Walsh MY, Bingham EA. Irvine AD, et al. Among authors: bingham ea. Arch Dermatol. 1997 Apr;133(4):474-7. doi: 10.1001/archderm.133.4.474. Arch Dermatol. 1997. PMID: 9126011

6

Mutation analysis in Irish families with glomuvenous malformations.

O'Hagan AH, Moloney FJ, Buckley C, Bingham EA, Walsh MY, McKenna KE, McGibbon D, Hughes AE. O'Hagan AH, et al. Among authors: bingham ea. Br J Dermatol. 2006 Mar;154(3):450-2. doi: 10.1111/j.1365-2133.2005.07041.x. Br J Dermatol. 2006. PMID: 16445774

7

Carney complex: report of a kindred with predominantly cutaneous manifestations.

Armstrong DK, Irvine AD, Handley JM, Walsh MY, Hadden DR, Bingham EA. Armstrong DK, et al. Among authors: bingham ea. Br J Dermatol. 1997 Apr;136(4):578-82. Br J Dermatol. 1997. PMID: 9155962

8

Evidence for a second genetic locus in Carney complex.

Irvine AD, Armstrong DK, Bingham EA, Hadden DR, Nevin NC, Hughes AE. Irvine AD, et al. Among authors: bingham ea. Br J Dermatol. 1998 Oct;139(4):572-6. doi: 10.1046/j.1365-2133.1998.02450.x. Br J Dermatol. 1998. PMID: 9892898

9

Miliary neonatal hemangiomatosis with fulminant heart failure and cardiac septal hypertrophy in two infants.

O'Hagan AH, Irvine AD, Sands A, O'Donaghue D, Casey F, Bingham EA. O'Hagan AH, et al. Among authors: bingham ea. Pediatr Dermatol. 2004 Jul-Aug;21(4):469-72. doi: 10.1111/j.0736-8046.2004.21411.x. Pediatr Dermatol. 2004. PMID: 15283793

10

Linkage of epidermolysis bullosa simplex to keratin gene loci.

McKenna KE, Hughes AE, Bingham EA, Nevin NC. McKenna KE, et al. Among authors: bingham ea. J Med Genet. 1992 Aug;29(8):568-70. doi: 10.1136/jmg.29.8.568. J Med Genet. 1992. PMID: 1381443 Free PMC article.

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