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Constitutive fragile sites in fra(X) individuals.
Jenkins EC, Lele KP, Krawczun MS, Gross AC, Duncan CJ, Brown WT. Jenkins EC, et al. Am J Med Genet. 1988 May-Jun;30(1-2):429-34. doi: 10.1002/ajmg.1320300144. Am J Med Genet. 1988. PMID: 3052066
Prenatal diagnosis and carrier screening for fragile X by PCR.
Brown WT, Nolin S, Houck G Jr, Ding X, Glicksman A, Li SY, Stark-Houck S, Brophy P, Duncan C, Dobkin C, Jenkins E. Brown WT, et al. Am J Med Genet. 1996 Jul 12;64(1):191-5. doi: 10.1002/(SICI)1096-8628(19960712)64:1<191::AID-AJMG34>3.0.CO;2-G. Am J Med Genet. 1996. PMID: 8826474
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. Am J Med Genet. 1988 May-Jun;30(1-2):329-36. doi: 10.1002/ajmg.1320300133. Am J Med Genet. 1988. PMID: 2972205
Folic acid treatment of fragile X males: a further study.
Fisch GS, Cohen IL, Gross AC, Jenkins V, Jenkins EC, Brown WT. Fisch GS, et al. Among authors: jenkins v, jenkins ec. Am J Med Genet. 1988 May-Jun;30(1-2):393-9. doi: 10.1002/ajmg.1320300139. Am J Med Genet. 1988. PMID: 3052065 Clinical Trial.
In situ nick translation of the fragile X region.
Nolin SL, Jenkins EC, Brown WT, Dobkin CS. Nolin SL, et al. Among authors: jenkins ec. Am J Med Genet. 1988 May-Jun;30(1-2):443-50. doi: 10.1002/ajmg.1320300146. Am J Med Genet. 1988. PMID: 3052067
Multilocus analysis of the fragile X syndrome.
Brown WT, Gross A, Chan C, Jenkins EC, Mandel JL, Oberlé I, Arveiler B, Novelli G, Thibodeau S, Hagerman R, et al. Brown WT, et al. Among authors: jenkins ec. Hum Genet. 1988 Mar;78(3):201-5. doi: 10.1007/BF00291662. Hum Genet. 1988. PMID: 3162224
221 results