Flanagan S - Search Results

1

Clinical findings in a patient with FGFR1 P252R mutation and comparison with the literature.

Roscioli T, Flanagan S, Kumar P, Masel J, Gattas M, Hyland VJ, Glass IA. Roscioli T, et al. Among authors: flanagan s. Am J Med Genet. 2000 Jul 3;93(1):22-8. doi: 10.1002/1096-8628(20000703)93:1<22::aid-ajmg5>3.0.co;2-u. Am J Med Genet. 2000. PMID: 10861678 Review.

2

Somatic and germline mosaicism for a R248C missense mutation in FGFR3, resulting in a skeletal dysplasia distinct from thanatophoric dysplasia.

Hyland VJ, Robertson SP, Flanagan S, Savarirayan R, Roscioli T, Masel J, Hayes M, Glass IA. Hyland VJ, et al. Among authors: flanagan s. Am J Med Genet A. 2003 Jul 15;120A(2):157-68. doi: 10.1002/ajmg.a.20012. Am J Med Genet A. 2003. PMID: 12833394

3

Premature calvarial synostosis and epidermal hyperplasia (Beare-Stevenson syndrome-like anomalies) resulting from a P250R missense mutation in the gene encoding fibroblast growth factor receptor 3.

Roscioli T, Flanagan S, Mortimore RJ, Kumar P, Weedon D, Masel J, Lewandowski R, Hyland V, Glass IA. Roscioli T, et al. Among authors: flanagan s. Am J Med Genet. 2001 Jul 1;101(3):187-94. doi: 10.1002/ajmg.1369. Am J Med Genet. 2001. PMID: 11424131

4

Prevalence of mutations in the short stature homeobox containing gene (SHOX) in Madelung deformity of childhood.

Flanagan SF, Munns CF, Hayes M, Williams B, Berry M, Vickers D, Rao E, Rappold GA, Batch JA, Hyland VJ, Glass IA. Flanagan SF, et al. J Med Genet. 2002 Oct;39(10):758-63. doi: 10.1136/jmg.39.10.758. J Med Genet. 2002. PMID: 12362035 Free PMC article. No abstract available.

5

Histopathological analysis of Leri-Weill dyschondrosteosis: disordered growth plate.

Munns CF, Glass IA, LaBrom R, Hayes M, Flanagan S, Berry M, Hyland VJ, Batch JA, Philips GE, Vickers D. Munns CF, et al. Among authors: flanagan s. Hand Surg. 2001 Jul;6(1):13-23. doi: 10.1142/s0218810401000424. Hand Surg. 2001. PMID: 11677662

6

Familial growth and skeletal features associated with SHOX haploinsufficiency.

Munns CF, Glass IA, Flanagan S, Hayes M, Williams B, Berry M, Vickers D, O'Rourke P, Rao E, Rappold GA, Hyland VJ, Batch JA. Munns CF, et al. Among authors: flanagan s. J Pediatr Endocrinol Metab. 2003 Sep;16(7):987-96. doi: 10.1515/jpem.2003.16.7.987. J Pediatr Endocrinol Metab. 2003. PMID: 14513875

7

CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leucoencephalopathy): an Australian perspective.

Chuah TL, Tan KM, Flanagan S, Hyland V, Sullivan AA, Henderson R, MacMillan J, Lander C. Chuah TL, et al. Among authors: flanagan s. J Clin Neurosci. 2001 Sep;8(5):404-6. doi: 10.1054/jocn.2000.0848. J Clin Neurosci. 2001. PMID: 11535004

8

Isocitrate dehydrogenase mutations in diffuse gliomas: clinical and aetiological implications.

Gupta R, Webb-Myers R, Flanagan S, Buckland ME. Gupta R, et al. Among authors: flanagan s. J Clin Pathol. 2011 Oct;64(10):835-44. doi: 10.1136/jclinpath-2011-200227. Epub 2011 Jul 12. J Clin Pathol. 2011. PMID: 21752797 Review.

9

Expanding the spectrum of IDH1 mutations in gliomas.

Gupta R, Flanagan S, Li CC, Lee M, Shivalingham B, Maleki S, Wheeler HR, Buckland ME. Gupta R, et al. Among authors: flanagan s. Mod Pathol. 2013 May;26(5):619-25. doi: 10.1038/modpathol.2012.210. Epub 2013 Jan 11. Mod Pathol. 2013. PMID: 23307057 Free article.

10

Promoter Methylation Analysis of IDH Genes in Human Gliomas.

Flanagan S, Lee M, Li CC, Suter CM, Buckland ME. Flanagan S, et al. Front Oncol. 2012 Dec 19;2:193. doi: 10.3389/fonc.2012.00193. eCollection 2012. Front Oncol. 2012. PMID: 23267435 Free PMC article.

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