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2011
H. - S. Lee, Kim, M. J., Lim, C. K., Cho, J. W., Song, I. O., and Kang, I. S., Multiple displacement amplification for preimplantation genetic diagnosis of fragile X syndrome, vol. 10. pp. 2851-2859, 2011.
Apessos A, Abou-Sleiman PM, Harper JC and Delhanty JD (2001). Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers. Prenat. Diagn. 21: 504-511. http://dx.doi.org/10.1002/pd.111 PMid:11438958 Burlet P, Frydman N, Gigarel N, Kerbrat V, et al. (2006). Multiple displacement amplification improves PGD for fragile X syndrome. Mol. Hum. Reprod. 12: 647-652. http://dx.doi.org/10.1093/molehr/gal069 PMid:16896070 de Vries BB, van den Ouweland AM, Mohkamsing S, Duivenvoorden HJ, et al. (1997). Screening and diagnosis for the fragile X syndrome among the mentally retarded: an epidemiological and psychological survey. Collaborative fragile X study group. Am. J. Hum. Genet. 61: 660-667. http://dx.doi.org/10.1086/515496 Dean FB, Hosono S, Fang L, Wu X, et al. (2002). Comprehensive human genome amplification using multiple displacement amplification. Proc. Natl. Acad. Sci. U. S. A. 99: 5261-5266. http://dx.doi.org/10.1073/pnas.082089499 PMid:11959976    PMCid:122757 Grace J, El-Toukhy T, Scriven P, Ogilvie C, et al. (2006). Three hundred and thirty cycles of preimplantation genetic diagnosis for serious genetic disease: clinical considerations affecting outcome. BJOG 113: 1393-1401. http://dx.doi.org/10.1111/j.1471-0528.2006.01143.x Gyapay G, Morissette J, Vignal A, Dib C, et al. (1994). The 1993-94 genethon human genetic linkage map. Nat. Genet. 7: 246-339. http://dx.doi.org/10.1038/ng0694supp-246 PMid:7545953 Hagerman RJ (1996). Physical and Behavioral Phenotype. In: Fragile X Syndrome: Diagnosis, Treatment and Research (Hagerman RJ and Silverman AC, eds.). John Hopkins University Press, Baltimore and London, 3-87. Handyside AH, Robinson MD, Simpson RJ, Omar MB, et al. (2004). Isothermal whole genome amplification from single and small numbers of cells: a new era for preimplantation genetic diagnosis of inherited disease. Mol. Hum. Reprod. 10: 767-772. http://dx.doi.org/10.1093/molehr/gah101 PMid:15322224 Hellani A, Coskun S, Benkhalifa M, Tbakhi A, et al. (2004). Multiple displacement amplification on single cell and possible PGD applications. Mol. Hum. Reprod. 10: 847-852. http://dx.doi.org/10.1093/molehr/gah114 PMid:15465849 Hellani A, Coskun S, Tbakhi A and Al-Hassan S (2005). Clinical application of multiple displacement amplification in preimplantation genetic diagnosis. Reprod. Biomed. Online 10: 376-380. http://dx.doi.org/10.1016/S1472-6483(10)61799-3 Kyu LC, Hyun JJ, Mi MD, Lee HS, et al. (2004). Efficacy and clinical outcome of preimplantation genetic diagnosis using FISH for couples of reciprocal and Robertsonian translocations: the Korean experience. Prenat. Diagn. 24: 556-561. http://dx.doi.org/10.1002/pd.923 PMid:15300749 Lee HS, Choi HW, Lim CK, Park SY, et al. (2005). Efficacy of duplex-nested PCR and fluorescent PCR in the preimplantation genetic diagnosis for Duchenne muscular dystrophy. Korean J. Fertil. Steril. 32: 17-26. Lee HS, Choi HW, Lim CK, Koong MK, et al. (2006). Identification of a novel single nucleotide polymorphism of HADHA gene at a referred primer-binding site during pre-diagnostic tests for preimplantation genetic diagnosis. J. Korean Med. Sci. 21: 794-799. http://dx.doi.org/10.3346/jkms.2006.21.5.794 PMid:17043408    PMCid:2721985 Lee HS, Jun JH, Choi HW, Lim CK, et al. (2007). Preimplantation genetic diagnosis for ornithine transcarbamylase deficiency by simultaneous analysis of duplex-nested PCR and fluorescence in situ hybridization: a case report. J. Korean Med. Sci. 22: 572-576. http://dx.doi.org/10.3346/jkms.2007.22.3.572 PMid:17596675    PMCid:2693659 Lledo B, Bernabeu R, Ten J, Galan FM, et al. (2007). Preimplantation genetic diagnosis of X-linked adrenoleukodystrophy with gender determination using multiple displacement amplification. Fertil. Steril. 88: 1327-1333. http://dx.doi.org/10.1016/j.fertnstert.2007.01.034 PMid:17498713 Oostra BA and Chiurazzi P (2001). The fragile X gene and its function. Clin. Genet. 60: 399-408. http://dx.doi.org/10.1034/j.1399-0004.2001.600601.x Richards RI, Holman K, Kozman H, Kremer E, et al. (1991). Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site. J. Med. Genet. 28: 818-823. http://dx.doi.org/10.1136/jmg.28.12.818 PMid:1757956    PMCid:1017157 Sermon K, Seneca S, Vanderfaeillie A, Lissens W, et al. (1999). Preimplantation diagnosis for fragile X syndrome based on the detection of the non-expanded paternal and maternal CGG. Prenat. Diagn. 19: 1223-1230. http://dx.doi.org/10.1002/(SICI)1097-0223(199912)19:13<1223::AID-PD724>3.0.CO;2-0 Telenius H, Carter NP, Bebb CE, Nordenskjold M, et al. (1992). Degenerate oligonucleotide-primed PCR: general amplification of target DNA by a single degenerate primer. Genomics 13: 718-725. http://dx.doi.org/10.1016/0888-7543(92)90147-K Turner G, Webb T, Wake S and Robinson H (1996). Prevalence of fragile X syndrome. Am. J. Med. Genet. 64: 196-197. http://dx.doi.org/10.1002/(SICI)1096-8628(19960712)64:1<196::AID-AJMG35>3.0.CO;2-G Zhang L, Cui X, Schmitt K, Hubert R, et al. (1992). Whole genome amplification from a single cell: implications for genetic analysis. Proc. Natl. Acad. Sci. U. S. A. 89: 5847-5851. http://dx.doi.org/10.1073/pnas.89.13.5847
X. Wan, Li, J., Kim, M. J., Kang, T. H., Jin, B. R., and Kim, I., Population genetic structure of the migratory rice leaf roller, Cnaphalocrocis medinalis (Lepidoptera: Pyralidae), inferred from the mitochondrial A+T-rich region and nuclear ITS2 sequences, vol. 10, pp. 273-294, 2011.
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