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[1] D. J. Driscoll,et al. Prader-Willi syndrome. , 1984, Current problems in pediatrics.
[2] O. el-Maarri,et al. Epimutations in Prader-Willi and Angelman syndromes: a molecular study of 136 patients with an imprinting defect. , 2003, American journal of human genetics.
[3] J. Vizmanos,et al. [Prader-Willi syndrome large deletion on two brothers. Is this the exception that confirm the rule?]. , 2001, Revista de neurología (Ed. impresa).
[4] H. Kokkonen,et al. An unexpected recurrence of Angelman syndrome suggestive of maternal germ-line mosaicism of del(15)(q11q13) in a Finnish family , 2000, Human Genetics.
[5] D. J. Driscoll,et al. DNA methylation analysis with respect to prenatal diagnosis of the Angelman and Prader–Willi syndromes and imprinting , 2000, Prenatal diagnosis.
[6] D. J. Driscoll,et al. Imprinting-mutation mechanisms in Prader-Willi syndrome. , 1999, American journal of human genetics.
[7] D. Ledbetter,et al. Methylation-specif ic PCR simplifies imprinting analysis , 1997, Nature genetics.
[8] D. Ledbetter,et al. Analysis of parent of origin specific DNA methylation at SNRPN and PW71 in tissues: implication for prenatal diagnosis. , 1996, Journal of medical genetics.
[9] D. J. Driscoll,et al. Familial cryptic translocation resulting in Angelman syndrome:implications for imprinting or location of the Angelman gene? , 1996, American journal of human genetics.
[10] D. J. Driscoll,et al. Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene. , 1996, American journal of human genetics.
[11] D. J. Driscoll,et al. Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome. , 1993, American journal of medical genetics.