Reply to Camprubí et al

[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.