References
- Burnside, R.D., Pasion, R., Mikhail, F.M., Carroll, A.J., Robin, N.H., Youngs, E.L., et al. (2011). Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay. Human Genetics, 130, 517–528.
- de Vree, P.J., Simon, M.E., van Dooren, M.F., Stoevelaar, G.H., Hilkmann, J.T., Rongen, M.A., et al. (2009). Application of molecular cytogenetic techniques to clarify apparently balanced complex chromosomal rearrangements in two patients with an abnormal phenotype: case report. Molecular Cytogenetics, 13, 2–15.
- Escudero, T., Estop, A., Ficher, J., & Munne, S. (2008). Preimplantation genetic diagnosis for complex chromosome rearrangements. American Journal of Medical Genetics Part A, 146, 1662–1669.
- Gardner, R.J.M. & Sutherland, G.R. (2004). Chromosome abnormalities and genetic Counselling. 3rd ed. New York: Oxford University Press Inc.
- Pai, G.S., Thomas, G.H., Mahoney, W., & Migeon, B.R. (1980). Complex chromosome rearrangements.Report of a new case and literature review. Clinical Genetics, 18, 436–444.
- Pellestor, F., Anahory, T., Lefort, G., Puechberty, J., Liehr, T., Hédon, B., & Sarda, P. (2011). Complex chromosomal rearrangements: origin and meiotic behavior. Human Reproduction Update, 17, 476–494.
- Sempere, A., Manchon, I., Palazon, I., Alcaraz, L., Perez, E., & Galan, F. (2011). Microdeleción 15q11.2(BP1-BP2).Un nuevo síndrome con expresividad variable. Anales de Pediatría (Barcelona), 75, 58–62.
- Tatton-Brown, K., Pilz, D.T., Orstavik, K.H., Patton, M., Barber, J.C.K., Collinson, M.N., et al. (2009). 15q overgrowth syndrome: a newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15q. American Journal of Medical Genetics Part A, 149A, 147–154.