Hayward RD - Search Results

1

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. Among authors: hayward rd. Nat Genet. 1995 Feb;9(2):165-72. doi: 10.1038/ng0295-165. Nat Genet. 1995. PMID: 7719344

2

Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes.

Rutland P, Pulleyn LJ, Reardon W, Baraitser M, Hayward R, Jones B, Malcolm S, Winter RM, Oldridge M, Slaney SF, et al. Rutland P, et al. Nat Genet. 1995 Feb;9(2):173-6. doi: 10.1038/ng0295-173. Nat Genet. 1995. PMID: 7719345

3

Spectrum of craniosynostosis phenotypes associated with novel mutations at the fibroblast growth factor receptor 2 locus.

Pulleyn LJ, Reardon W, Wilkes D, Rutland P, Jones BM, Hayward R, Hall CM, Brueton L, Chun N, Lammer E, Malcolm S, Winter RM. Pulleyn LJ, et al. Eur J Hum Genet. 1996;4(5):283-91. doi: 10.1159/000472215. Eur J Hum Genet. 1996. PMID: 8946174

4

Congenital cervical spinal fusion: a study in Apert syndrome.

Thompson DN, Slaney SF, Hall CM, Shaw D, Jones BM, Hayward RD. Thompson DN, et al. Among authors: hayward rd. Pediatr Neurosurg. 1996 Jul;25(1):20-7. doi: 10.1159/000121091. Pediatr Neurosurg. 1996. PMID: 9055330

5

The feet in Crouzon syndrome.

Anderson PJ, Hall CM, Evans RD, Jones BM, Hayward RD. Anderson PJ, et al. Among authors: hayward rd. J Craniofac Genet Dev Biol. 1997 Jan-Mar;17(1):43-7. J Craniofac Genet Dev Biol. 1997. PMID: 9211121

6

Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosis.

Reardon W, Wilkes D, Rutland P, Pulleyn LJ, Malcolm S, Dean JC, Evans RD, Jones BM, Hayward R, Hall CM, Nevin NC, Baraister M, Winter RM. Reardon W, et al. Among authors: hayward r. J Med Genet. 1997 Aug;34(8):632-6. doi: 10.1136/jmg.34.8.632. J Med Genet. 1997. PMID: 9279753 Free PMC article.

7

Acromelic frontonasal dysostosis.

Slaney SF, Goodman FR, Eilers-Walsman BL, Hall BD, Williams DK, Young ID, Hayward RD, Jones BM, Christianson AL, Winter RM. Slaney SF, et al. Among authors: hayward rd. Am J Med Genet. 1999 Mar 12;83(2):109-16. Am J Med Genet. 1999. PMID: 10190481 Review.

8

Further evidence from two families that craniofrontonasal dysplasia maps to Xp22.

Pulleyn LJ, Winter RM, Reardon W, McKeown C, Jones B, Hayward R, Evans R, Malcolm S. Pulleyn LJ, et al. Clin Genet. 1999 Jun;55(6):473-7. doi: 10.1034/j.1399-0004.1999.550613.x. Clin Genet. 1999. PMID: 10450866

9

Hand anomalies in Crouzon syndrome.

Anderson PJ, Hall CM, Evans RD, Jones BM, Hayward RD. Anderson PJ, et al. Among authors: hayward rd. Skeletal Radiol. 1997 Feb;26(2):113-5. doi: 10.1007/s002560050203. Skeletal Radiol. 1997. PMID: 9060103

10

Frontonasal dysplasia with optic disc anomalies and other midline craniofacial defects: a report of six cases.

Lees MM, Hodgkins P, Reardon W, Taylor D, Stanhope R, Jones B, Hayward R, Hockley AD, Baraitser M, Winter RM. Lees MM, et al. Clin Dysmorphol. 1998 Jul;7(3):157-62. doi: 10.1097/00019605-199807000-00001. Clin Dysmorphol. 1998. PMID: 9689987 Review.

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