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Page 1
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
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.
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
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
222 results