Associated Papers
Causative and common PHOX2B variants define a broad phenotypic spectrum.
Bachetti T et al.
Clinical Genetics, 2020
Prevalence and functional consequence of PHOX2B mutations in neuroblastoma.
Raabe EH et al.
Oncogene, 2008
Methylation-associated PHOX2B gene silencing is a rare event in human neuroblastoma.
de Pontual L et al.
European Journal of Cancer (oxford, England : 1990), 2007
Sudden infant death syndrome: Case-control frequency differences in paired like homeobox (PHOX) 2B gene.
Rand CM et al.
American Journal of Medical Genetics. Part A, 2006
PHOX2B analysis in non-syndromic neuroblastoma cases shows novel mutations and genotype-phenotype associations.
McConville C et al.
American Journal of Medical Genetics. Part A, 2006
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