4Haw-Smith C, Rendon R, Rickman I, et al. Microarray based comparative genomic hybridization ( array-CGH ) detects submicroscopic chromosomal deletions and duplications in patients with learning disability mental retardation and dysmorphic features. J Med Genet, 2004,41 : 241-248.
6Minoeherhomji S, Athalye AS, Madon PF, et al. A case-control study identifying chromosomal polymorphic variations as forms of epigenetic alterations associated with the infertility phenotype. Fertil Steril. 2009,92 : 88-95.
7Akkari Y, Lawce H, Kelson S. Y chromosome heterochromatin of differing lengths in two cell populations of the same individual. Prenat Diagn, 2005,25: 304-306.
8Jeong SY, Kim BY, Yu JE. De novo pericentric inversion of chromosome 9 in congenital anomaly. Yonsei Med J, 2010, 51: 775-780.
7Tho SPT. Chromosome polymorphism in couple with reproductive failtire and subsequent pregnancy outcome. Fertil Steril, 1982, 38: 688-689.
8沈婉英.汉族男性Y染色体相对长度152例分析[J].遗传与疾病,1990,7(1):37-38.
9Patricla DE,Preri,Dirceu H,et al.A cost-effective screening test for detecting AZF microdeletions on the humen Y chromosome[J].Genetic Testing,2002,6(3):185.
10Kleiman SE,Yogel,Paz G,et al.The prognostic value of the site andextent of Y chromosome microdeletion on spermatogenesis[J].Harefsh,2002,141:178.
9FanH Christina/HC ,Blumenfeld,Yair JArJ;Chitkara,Usha/U;Hudgins,Louanne/L;Quake,Stephen R/SR;Proceedings of theNational Academy of Sciences of the United States of America,2008,105(42):16266-71.
10ChenHZ, Chiu RW,Sun H,et al.Noninvasive prenatal diagnosis of fetal trisomy 18 and trisomy 13 by maternal plasma DNA sequencing[J].PLoS One,2011,6(7):e21791.
