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References
Amiel J, Laudier B, Attie-Bitach T, Trang H, de Pontual L, Gener B et al. (2003) Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome. Nat Genet 33:459–461
Blatt J, Olshan AF, Lee PA, Ross JL (1997) Neuroblastoma and related tumors in Turner's syndrome (published erratum appears in J Pediatr 1998, 133:312). J Pediatr 131:666–670
Dodge HJ, Benner MC (1945) Neuroblastoma of the adrenal medulla in siblings. Rocky Mt Med 42:35–38
Furuta S, Ohira M, Machida T, Hamano S, Nakagawara A (2000) Analysis of loss of heterozygosity at 16p12–p13 (familial neuroblastoma locus) in 470 neuroblastomas including both sporadic and mass screening tumors. Med Pediatr Oncol 35:531–533
Knudson AG Jr, Strong LC (1972) Mutation and cancer: neuroblastoma and pheochromocytoma. Am J Hum Genet 24:514–532
Kushner BH, Gilbert F, Helson L (1986) Familial neuroblastoma. Case reports, literature review, and etiologic considerations. Cancer 57:1887–1893
Lemire EG, Chodirker BN, Williams GJ, Seargeant LE, Israels SJ, Phillips SM et al (1998) Familial neuroblastoma: report of a kindred with later age at presentation. J Pediatr Hematol Oncol 20:489–493
Maris JM, Brodeur GM (2001) Genetics of neuroblastoma. In: Cowell JK (ed) Molecular genetics of cancer, 2nd edn. BIOS, Oxford, pp 335–361
Maris JM, Kyemba SM, Rebbeck TR, White PS, Sulman EP, Jensen SJ et al. (1996) Familial predisposition to neuroblastoma does not map to chromosome band 1p36. Cancer Res 56:3421–3425
Maris JM, Chatten J, Meadows AT, Biegel JA, Brodeur GM (1997) Familial neuroblastoma: a three generation pedigree and a further association with Hirschsprung disease. Med Pediatr Oncol 28:1–5
Maris JM, Weiss MJ, Mosse Y, Hii G, Guo C, White PS et al. (2002) Evidence for a hereditary neuroblastoma predisposition locus at chromosome 16p12–13. Cancer Res 62:6651–6658
Maris JM, Mosse Y, Hii G, Dahia P (2003) Familial neuroblastoma: Further evidence for linkage to 16p13 and refinement of the HNB1 locus. Med Pediatr Oncol 41:293
Martinsson T, Sjoberg RM, Hedborg F, Kogner P (1997) Homozygous deletion of the neurofibromatosis-1 gene in the tumor of a patient with neuroblastoma. Cancer Genet Cytogenet 95:183–189
Mosse Y, Greshock J, King A, Khazi D, Weber BL, Maris JM (2003) Identification and high-resolution mapping of a constitutional 11q deletion in an infant with multifocal neuroblastoma. Lancet Oncol 4:769–771
Origone P, Defferrari R, Mazzocco K, Lo Cunsolo C, Bernardi B de, Tonini GP (2003) Homozygous inactivation of NF1 gene in a patient with familial NF1 and disseminated neuroblastoma. Am J Med Genet 118A:309–313
Perri P, Longo L, Cusano R, McConville CM, Rees SA, Devoto M et al. (2002) Weak linkage at 4p16 to predisposition for human neuroblastoma. Oncogene 21:8356–8360
Sariola H, Saarma M (2003) Novel functions and signalling pathways for GDNF. J Cell Sci 116:3855–3862
Satge D, Sasco AJ, Carlsen NL, Stiller CA, Rubie H, Hero B et al. (1998) A lack of neuroblastoma in Down syndrome: a study from 11 European countries. Cancer Res 58:448–452
Satge D, Moore SW, Stiller CA, Niggli FK, Pritchard-Jones K, Bown N et al.(2003) Abnormal constitutional karyotypes in patients with neuroblastoma: a report of four new cases and review of 47 others in the literature. Cancer Genet Cytogenet 147:89–98
Shojaei-Brosseau T, Chompret A, Abel A, de Vathaire F, Raquin MA, Brugieres L et al (2004) Genetic epidemiology of neuroblastoma: a study of 426 cases at the Institut Gustave-Roussy in France. Pediatr Blood Cancer 42:99–105
Takahashi M (2001) The GDNF/RET signaling pathway and human diseases. Cytokine Growth Factor Rev 12:361–73
Tonini GP, McConville C, Cusano R, Rees SA, Dagnino M, Longo L et al. (2001) Exclusion of candidate genes and chromosomal regions in familial neuroblastoma. Int J Mol Med 7:85–89
Verloes A, Elmer C, Lacombe D, Heinrichs C, Rebuffat E, Demarquez JL et al. (1993) Ondine-Hirschsprung syndrome (Haddad syndrome). Further delineation in two cases and review of the literature. Eur J Pediatr 152:75–77
White PS, Thompson PM, Seifried BA, Sulman EP, Jensen SJ, Guo C et al. (2001) Detailed molecular analysis of 1p36 in neuroblastoma. Med Pediatr Oncol 36:37–41
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Maris, J.M., Brodeur, G.M. (2005). Genetics. In: Cheung, NK.V., Cohn, S.L. (eds) Neuroblastoma. Pediatric Oncology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/3-540-26616-X_3
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DOI: https://doi.org/10.1007/3-540-26616-X_3
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