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Variable human phenotype associated with novel deletions of the PHOX2B gene.
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Variable human phenotype associated with novel deletions of the PHOX2B gene.
Variable human phenotype associated with novel deletions of the PHOX2B gene. Pediatr Pulmonol. 2012 Feb; 47(2):153-61.
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PubMed
subject areas
Adult
Child, Preschool
DNA Mutational Analysis
Exons
Female
Gene Deletion
Gene Duplication
Hirschsprung Disease
Homeodomain Proteins
Humans
Hypoventilation
Infant
Male
Phenotype
Sleep Apnea, Central
Transcription Factors
authors with profiles
Elizabeth Berry-Kravis