Germline PHOX2B Mutation in Hereditary Neuroblastoma
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
Reference12 articles.
1. Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome;Amiel;Nat Genet,2003
2. Phox2 genes: from patterning to connectivity;Brunet;Curr Opin Genet Dev,2002
3. Segregation at three loci explains familial and population risk in Hirschsprung disease;Gabriel;Nat Genet,2002
4. Coexistent neuroblastoma and Hirschsprung’s disease: another manifestation of the neurocristopathy?;Gaisie;Pediatr Radiol,1979
5. Molecular biology of neuroblastoma;Maris;J Clin Oncol,1999
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2. Immunohistochemistry study of PHOX2B expression in Hirschsprung's disease allied disorders;Journal of Pediatric Surgery Open;2024-07
3. Genetic identification of medullary neurons underlying congenital hypoventilation;Science Advances;2024-06-21
4. Neuroblastoma susceptibility and association of N7-methylguanosine modification gene polymorphisms: multi-center case-control study;Pediatric Research;2024-06-13
5. Neuroblastoma Predisposition and Surveillance—An Update from the 2023 AACR Childhood Cancer Predisposition Workshop;Clinical Cancer Research;2024-06-11
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