Wilkie AO - Search Results

1

Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects.

Mavrogiannis LA, Antonopoulou I, Baxová A, Kutílek S, Kim CA, Sugayama SM, Salamanca A, Wall SA, Morriss-Kay GM, Wilkie AO. Mavrogiannis LA, et al. Among authors: wilkie ao. Nat Genet. 2001 Jan;27(1):17-8. doi: 10.1038/83703. Nat Genet. 2001. PMID: 11137991

2

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

3

Functions of fibroblast growth factors and their receptors.

Wilkie AO, Morriss-Kay GM, Jones EY, Heath JK. Wilkie AO, et al. Curr Biol. 1995 May 1;5(5):500-7. doi: 10.1016/s0960-9822(95)00102-3. Curr Biol. 1995. PMID: 7583099 Free article. Review.

4

Mutations in the third immunoglobulin domain of the fibroblast growth factor receptor-2 gene in Crouzon syndrome.

Oldridge M, Wilkie AO, Slaney SF, Poole MD, Pulleyn LJ, Rutland P, Hockley AD, Wake MJ, Goldin JH, Winter RM, et al. Oldridge M, et al. Among authors: wilkie ao. Hum Mol Genet. 1995 Jun;4(6):1077-82. doi: 10.1093/hmg/4.6.1077. Hum Mol Genet. 1995. PMID: 7655462

5

The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation.

Flint J, Wilkie AO, Buckle VJ, Winter RM, Holland AJ, McDermid HE. Flint J, et al. Among authors: wilkie ao. Nat Genet. 1995 Feb;9(2):132-40. doi: 10.1038/ng0295-132. Nat Genet. 1995. PMID: 7719339

6

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome.

Wilkie AO, Slaney SF, Oldridge M, Poole MD, Ashworth GJ, Hockley AD, Hayward RD, David DJ, Pulleyn LJ, Rutland P, et al. Wilkie AO, et al. Nat Genet. 1995 Feb;9(2):165-72. doi: 10.1038/ng0295-165. Nat Genet. 1995. PMID: 7719344

7

A gene map of congenital malformations.

Wilkie AO, Amberger JS, McKusick VA. Wilkie AO, et al. J Med Genet. 1994 Jul;31(7):507-17. doi: 10.1136/jmg.31.7.507. J Med Genet. 1994. PMID: 7966186 Free PMC article. Review.

8

Exclusive paternal origin of new mutations in Apert syndrome.

Moloney DM, Slaney SF, Oldridge M, Wall SA, Sahlin P, Stenman G, Wilkie AO. Moloney DM, et al. Among authors: wilkie ao. Nat Genet. 1996 May;13(1):48-53. doi: 10.1038/ng0596-48. Nat Genet. 1996. PMID: 8673103

9

Craniosynostosis: novel insights into pathogenesis and treatment.

Wilkie AO, Wall SA. Wilkie AO, et al. Curr Opin Neurol. 1996 Apr;9(2):146-52. Curr Opin Neurol. 1996. PMID: 8782984 Review.

10

Prevalence of Pro250Arg mutation of fibroblast growth factor receptor 3 in coronal craniosynostosis.

Moloney DM, Wall SA, Ashworth GJ, Oldridge M, Glass IA, Francomano CA, Muenke M, Wilkie AO. Moloney DM, et al. Among authors: wilkie ao. Lancet. 1997 Apr 12;349(9058):1059-62. doi: 10.1016/s0140-6736(96)09082-4. Lancet. 1997. PMID: 9107244

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