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Fragile X-related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study.
Inaba Y, Herlihy AS, Schwartz CE, Skinner C, Bui QM, Cobb J, Shi EZ, Francis D, Arvaj A, Amor DJ, Pope K, Wotton T, Cohen J, Hewitt JK, Hagerman RJ, Metcalfe SA, Hopper JL, Loesch DZ, Slater HR, Godler DE. Inaba Y, et al. Among authors: hagerman rj. Genet Med. 2013 Apr;15(4):290-8. doi: 10.1038/gim.2012.134. Epub 2012 Oct 11. Genet Med. 2013. PMID: 23060046 Free article.
Fragile X checklist.
Hagerman RJ, Amiri K, Cronister A. Hagerman RJ, et al. Am J Med Genet. 1991 Feb-Mar;38(2-3):283-7. doi: 10.1002/ajmg.1320380223. Am J Med Genet. 1991. PMID: 2018072
Institutional screening for the fragile X syndrome.
Hagerman R, Berry R, Jackson AW 3rd, Campbell J, Smith AC, McGavran L. Hagerman R, et al. Am J Dis Child. 1988 Nov;142(11):1216-21. doi: 10.1001/archpedi.1988.02150110094028. Am J Dis Child. 1988. PMID: 3177330
Cognitive profiles of boys with the fragile X syndrome.
Kemper MB, Hagerman RJ, Altshul-Stark D. Kemper MB, et al. Among authors: hagerman rj. Am J Med Genet. 1988 May-Jun;30(1-2):191-200. doi: 10.1002/ajmg.1320300118. Am J Med Genet. 1988. PMID: 3177444
Cognitive variability in the fragile X syndrome.
Chudley AE, de von Flindt R, Hagerman RJ. Chudley AE, et al. Among authors: hagerman rj. Am J Med Genet. 1987 Sep;28(1):13-5. doi: 10.1002/ajmg.1320280103. Am J Med Genet. 1987. PMID: 3674106 No abstract available.
Autism in fragile X females.
Hagerman RJ, Chudley AE, Knoll JH, Jackson AW 3rd, Kemper M, Ahmad R. Hagerman RJ, et al. Am J Med Genet. 1986 Jan-Feb;23(1-2):375-80. doi: 10.1002/ajmg.1320230129. Am J Med Genet. 1986. PMID: 3953655
578 results