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Localization of chromosome 21 probes by in situ hybridization.
Brown WT, Devine EA, Nolin SL, Houck GE Jr, Jenkins EC. Brown WT, et al. Among authors: nolin sl. Ann N Y Acad Sci. 1985;450:69-83. doi: 10.1111/j.1749-6632.1985.tb21484.x. Ann N Y Acad Sci. 1985. PMID: 3160293 No abstract available.
In situ nick translation of the fragile X region.
Nolin SL, Jenkins EC, Brown WT, Dobkin CS. Nolin SL, et al. Am J Med Genet. 1988 May-Jun;30(1-2):443-50. doi: 10.1002/ajmg.1320300146. Am J Med Genet. 1988. PMID: 3052067
Reverse mutations in the fragile X syndrome.
Brown WT, Houck GE Jr, Ding X, Zhong N, Nolin S, Glicksman A, Dobkin C, Jenkins EC. Brown WT, et al. Am J Med Genet. 1996 Aug 9;64(2):287-92. doi: 10.1002/(SICI)1096-8628(19960809)64:2<287::AID-AJMG11>3.0.CO;2-B. Am J Med Genet. 1996. PMID: 8844067
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. Am J Med Genet. 1991 Feb-Mar;38(2-3):251-5. doi: 10.1002/ajmg.1320380218. Am J Med Genet. 1991. PMID: 2018068
Mosaicism in fragile X affected males.
Nolin SL, Glicksman A, Houck GE Jr, Brown WT, Dobkin CS. Nolin SL, et al. Am J Med Genet. 1994 Jul 15;51(4):509-12. doi: 10.1002/ajmg.1320510444. Am J Med Genet. 1994. PMID: 7943031
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
46 results