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Neurofibromatosis type 1 is a genetic skeletal disorder.
Stevenson DA, Viskochil DH, Carey JC. Stevenson DA, et al. Among authors: carey jc. Am J Med Genet A. 2007 Sep 1;143A(17):2082-3; author reply 2084. doi: 10.1002/ajmg.a.31758. Am J Med Genet A. 2007. PMID: 17702004 No abstract available.
Nosological considerations of the neurofibromatoses.
Viskochil D, Carey JC. Viskochil D, et al. Among authors: carey jc. J Dermatol. 1992 Nov;19(11):873-80. doi: 10.1111/j.1346-8138.1992.tb03798.x. J Dermatol. 1992. PMID: 1293176
The NF1 translocation breakpoint region.
O'Connell P, Cawthon RM, Viskochil D, White R, Carey JC, Buchberg AM. O'Connell P, et al. Among authors: carey jc. Ann N Y Acad Sci. 1991;615:319-31. doi: 10.1111/j.1749-6632.1991.tb37774.x. Ann N Y Acad Sci. 1991. PMID: 1903909 Review.
Current status of the human malformation map.
Carey JC, Viskochil DH. Carey JC, et al. Birth Defects Orig Artic Ser. 1996;30(1):13-34. Birth Defects Orig Artic Ser. 1996. PMID: 9125323 Review.
Descriptive analysis of tibial pseudarthrosis in patients with neurofibromatosis 1.
Stevenson DA, Birch PH, Friedman JM, Viskochil DH, Balestrazzi P, Boni S, Buske A, Korf BR, Niimura M, Pivnick EK, Schorry EK, Short MP, Tenconi R, Tonsgard JH, Carey JC. Stevenson DA, et al. Among authors: carey jc. Am J Med Genet. 1999 Jun 11;84(5):413-9. doi: 10.1002/(sici)1096-8628(19990611)84:5<413::aid-ajmg5>3.0.co;2-1. Am J Med Genet. 1999. PMID: 10360395
409 results