References
- Brambila Tapia AJ, Figuera L, Vázquez Cárdenas NA, Ramírez Torres V, Vázquez Velázquez AI, García Contreras C, RamírezDueñas ML. The variable phenotype in tetrasomy 18p syndrome. A propos of a subtle dysmorphic case. Genet Couns. 2010;21(3):277–83.
- Plaiasu V, Ochiana D, Motei G, Georgescu A. A rare chromosomal disorder—isochromosome 18p syndrome. Maedica 2011 Apr;6(2):132–6.
- Boyle J, Sangha K, Dill F, Robinson WP, Yong SL. Grandmaternal origin of an isochromosome 18p present in two maternal half-sisters. Am J Med Genet 2001 Jun;101(1):65–9.
- Chen CP, Ko TM, Su YN, Chern SR, Su JW, Chen YT, Town DD, Wang W. Prenatal diagnosis of mosaic tetrasomy 18p. Taiwan J ObstetGynecol 2012 Dec;51(4):625–29.
- Hsu LY, Yu MT, Richkind KE, Van Dyke DL, Crandall BF, Saxe DF, Khodr GS, Mennuti M, Stetten G, Miller WA, Priest JH. Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: a collaborative study. Prenat Diagn 1996 Jan;16(1):1–28.
- Abeliovich D, Dagan J, Levy A, Steinberg A, Zlotogora J. Isochromosome 18p in a mother and her child. Am J Med Genet 1993 Jun;46(4):392–93.
- Sebold C, Roeder E, Zimmerman M, Soileau B, Heard P, Carter E, Schatz M, White WA, Perry B, Reinker K, O'Donnell L, Lancaster J, Li J, Hasi M, Hill A, Pankratz L, Hale DE, Cody JD. Tetrasomy 18p: report of the molecular and clinical findings of 43 individuals. Am J Med Genet A 2010 Sep;152A(9):2164–72.
- Swingle HM, Ringdahl J, Mraz R, Patil S, Keppler-Noreuil K. Behavioral management of a long-term survivor with tetrasomy 18p. Am J Med Genet A 2006 Feb;140(3):276–80.
- Fraga MF, Ballestar E, Paz MF, Ropero S, Setien F, Ballestar ML, Heine-Suñer D, Cigudosa JC, Urioste M, Benitez J, Boix-Chornet M, Sanchez-Aguilera A, Ling C, Carlsson E, Poulsen P, Vaag A, Stephan Z, Spector TD, Wu YZ, Plass C, Esteller M. Epigenetic differences arise during the lifetime of monozygotic twins. Proc Natl Acad Sci U S A 2005 Jul;102(30):10604–9.