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A survey of FRAXE allele sizes in three populations.
Zhong N, Ju W, Curley D, Wang D, Pietrofesa J, Wu G, Shen Y, Pang C, Poon P, Liu X, Gou S, Kajanoja E, Ryynänen M, Dobkin C, Brown WT. Zhong N, et al. Am J Med Genet. 1996 Aug 9;64(2):415-9. doi: 10.1002/(SICI)1096-8628(19960809)64:2<415::AID-AJMG36>3.0.CO;2-G. Am J Med Genet. 1996. PMID: 8844095
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