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Splitting and lumping in the nosology of XLMR.
Stevenson RE. Stevenson RE. Am J Med Genet. 2000 Fall;97(3):174-82. doi: 10.1002/1096-8628(200023)97:3<174::AID-AJMG1034>3.0.CO;2-4. Am J Med Genet. 2000. PMID: 11449485 Review.
Duplication of distal 19q: clinical report and review.
Boyd E, Grass FS, Parke JC, Knutson K, Stevenson RE. Boyd E, et al. Among authors: stevenson re. Am J Med Genet. 1992 Feb 1;42(3):326-30. doi: 10.1002/ajmg.1320420314. Am J Med Genet. 1992. PMID: 1536172 Review.
MRX8: an X-linked mental retardation condition with linkage to Xq21.
Schwartz CE, May M, Huang T, Ledbetter D, Anderson G, Barker DF, Lubs HA, Arena F, Stevenson RE. Schwartz CE, et al. Among authors: stevenson re. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):467-74. doi: 10.1002/ajmg.1320430170. Am J Med Genet. 1992. PMID: 1605227
Allan-Herndon syndrome. I. Clinical studies.
Stevenson RE, Goodman HO, Schwartz CE, Simensen RJ, McLean WT Jr, Herndon CN. Stevenson RE, et al. Am J Hum Genet. 1990 Sep;47(3):446-53. Am J Hum Genet. 1990. PMID: 2393019 Free PMC article.
Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21.
Schwartz CE, Ulmer J, Brown A, Pancoast I, Goodman HO, Stevenson RE. Schwartz CE, et al. Among authors: stevenson re. Am J Hum Genet. 1990 Sep;47(3):454-8. Am J Hum Genet. 1990. PMID: 2393020 Free PMC article.
Fragile X syndrome and neoplasia.
Phelan MC, Stevenson RE, Collins JL, Trent HE 3rd. Phelan MC, et al. Among authors: stevenson re. Am J Med Genet. 1988 May-Jun;30(1-2):77-82. doi: 10.1002/ajmg.1320300106. Am J Med Genet. 1988. PMID: 2845782
Fragile X syndrome: growth, development, and intellectual function.
Prouty LA, Rogers RC, Stevenson RE, Dean JH, Palmer KK, Simensen RJ, Coston GN, Schwartz CE. Prouty LA, et al. Among authors: stevenson re. Am J Med Genet. 1988 May-Jun;30(1-2):123-42. doi: 10.1002/ajmg.1320300111. Am J Med Genet. 1988. PMID: 3177438
294 results