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Page 1
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
Molecular analysis of fragile X syndrome.
Nolin SL, Dobkin C, Brown WT. Nolin SL, et al. Curr Protoc Hum Genet. 2003 Nov;Chapter 9:Unit9.5. doi: 10.1002/0471142905.hg0905s38. Curr Protoc Hum Genet. 2003. PMID: 18428348
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
Fragile X founder effects and new mutations in Finland.
Zhong N, Kajanoja E, Smits B, Pietrofesa J, Curley D, Wang D, Ju W, Nolin S, Dobkin C, Ryynänen M, Brown WT. Zhong N, et al. Am J Med Genet. 1996 Jul 12;64(1):226-33. doi: 10.1002/(SICI)1096-8628(19960712)64:1<226::AID-AJMG41>3.0.CO;2-M. Am J Med Genet. 1996. PMID: 8826481
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
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
47 results