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Page 1
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
Familial Parry-Romberg disease.
Anderson PJ, Molony D, Haan E, David DJ. Anderson PJ, et al. Among authors: david dj. Int J Pediatr Otorhinolaryngol. 2005 May;69(5):705-8. doi: 10.1016/j.ijporl.2004.12.004. Int J Pediatr Otorhinolaryngol. 2005. PMID: 15850693
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
Craniofrontonasal dysostosis and the Poland anomaly.
Cantrell SB, Trott JA, Moore MH, David DJ. Cantrell SB, et al. Among authors: david dj. Am J Med Genet. 1994 Oct 1;52(4):498. doi: 10.1002/ajmg.1320520422. Am J Med Genet. 1994. PMID: 7747768 Review. No abstract available.
307 results