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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: dobkin c. Am J Med Genet. 1991 Feb-Mar;38(2-3):370-3. doi: 10.1002/ajmg.1320380242. Am J Med Genet. 1991. PMID: 1673313
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. Among authors: dobkin c. 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. Among authors: dobkin c. 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
115 results