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Recent experience in prenatal fra(X) detection.
Jenkins EC, Brown WT, Krawczun MS, Duncan CJ, Lele KP, Cantu ES, Schonberg S, Golbus MS, Sekhon GS, Stark S, et al. Jenkins EC, et al. Among authors: brown wt. Am J Med Genet. 1988 May-Jun;30(1-2):329-36. doi: 10.1002/ajmg.1320300133. Am J Med Genet. 1988. PMID: 2972205
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
Laboratory aspects of prenatal fra(X) detection.
Jenkins EC, Krawczun MS, Brooks SE, Brooks SL, Sherman SL, Brown WT. Jenkins EC, et al. Among authors: brown wt. Prog Clin Biol Res. 1991;368:27-42. Prog Clin Biol Res. 1991. PMID: 1835094 No abstract available.
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