Germline PHOX2B Mutation in Hereditary Neuroblastoma
Top Cited Papers
- 1 October 2004
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 75 (4), 727-730
- https://doi.org/10.1086/424530
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Linkage Analysis in Families with Recurrent NeuroblastomaAnnals of the New York Academy of Sciences, 2006
- PHOX2B mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndromeJournal of Medical Genetics, 2004
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- Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndromeNature Genetics, 2003
- Treatment of Neuroblastoma in Patients With Neurocristopathy SyndromesJournal of Pediatric Hematology/Oncology, 2003
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- Phox2 genes — from patterning to connectivityCurrent Opinion in Genetics & Development, 2002
- Segregation at three loci explains familial and population risk in Hirschsprung diseaseNature Genetics, 2002
- Coexistent neuroblastoma and Hirschsprung's disease ?Another manifestation of the neurocristopathy?Pediatric Radiology, 1979