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Page 1
Genotype and clinical care correlations in craniosynostosis: findings from a cohort of 630 Australian and New Zealand patients.
Roscioli T, Elakis G, Cox TC, Moon DJ, Venselaar H, Turner AM, Le T, Hackett E, Haan E, Colley A, Mowat D, Worgan L, Kirk EP, Sachdev R, Thompson E, Gabbett M, McGaughran J, Gibson K, Gattas M, Freckmann ML, Dixon J, Hoefsloot L, Field M, Hackett A, Kamien B, Edwards M, Adès LC, Collins FA, Wilson MJ, Savarirayan R, Tan TY, Amor DJ, McGillivray G, White SM, Glass IA, David DJ, Anderson PJ, Gianoutsos M, Buckley MF. Roscioli T, et al. Among authors: david dj. Am J Med Genet C Semin Med Genet. 2013 Nov;163C(4):259-70. doi: 10.1002/ajmg.c.31378. Epub 2013 Oct 11. Am J Med Genet C Semin Med Genet. 2013. PMID: 24127277
Mutation detection in FGFR2 craniosynostosis syndromes.
Hollway GE, Suthers GK, Haan EA, Thompson E, David DJ, Gecz J, Mulley JC. Hollway GE, et al. Among authors: david dj. Hum Genet. 1997 Feb;99(2):251-5. doi: 10.1007/s004390050348. Hum Genet. 1997. PMID: 9048930
Analysis of intracranial volume in apert syndrome genotypes.
Anderson PJ, Netherway DJ, Abbott AH, Cox T, Roscioli T, David DJ. Anderson PJ, et al. Among authors: david dj. Pediatr Neurosurg. 2004 Jul-Aug;40(4):161-4. doi: 10.1159/000081933. Pediatr Neurosurg. 2004. PMID: 15608488
Intracranial volume measurement of sagittal craniosynostosis.
Anderson PJ, Netherway DJ, McGlaughlin K, David DJ. Anderson PJ, et al. Among authors: david dj. J Clin Neurosci. 2007 May;14(5):455-8. doi: 10.1016/j.jocn.2006.07.001. Epub 2007 Feb 7. J Clin Neurosci. 2007. PMID: 17289391
305 results