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The fragile X syndrome.
Brown WT, Jenkins EC. Brown WT, et al. Mol Genet Med. 1992;2:39-66. doi: 10.1016/b978-0-12-462002-5.50007-8. Mol Genet Med. 1992. PMID: 1458226 Review. No abstract available.
Cytogenetically negative, linkage positive "fragile X" syndrome.
Sklower Brooks S, Cohen I, Ferrando C, Jenkins EC, Brown WT, Dobkin C. Sklower Brooks S, et al. Among authors: brown wt. Am J Med Genet. 1991 Feb-Mar;38(2-3):370-3. doi: 10.1002/ajmg.1320380242. Am J Med Genet. 1991. PMID: 1673313
SV40-transformed fragile (X) amniocytes.
Jenkins EC, Brooks SE, Stark-Houck SL, Duncan CJ, Brooks SL, Brown WT. Jenkins EC, et al. Among authors: brown wt. Am J Med Genet. 1991 Feb-Mar;38(2-3):464-6. doi: 10.1002/ajmg.1320380265. Am J Med Genet. 1991. PMID: 1850194
Fragile X screening program in New York State.
Nolin SL, Snider DA, Jenkins EC, Brown WT, Krawczun M, Stetka D, Houck G Jr, Dobkin CS, Strong G, Smith-Dobransky G, et al. Nolin SL, et al. Among authors: brown wt. Am J Med Genet. 1991 Feb-Mar;38(2-3):251-5. doi: 10.1002/ajmg.1320380218. Am J Med Genet. 1991. PMID: 2018068
398 results