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Adult identified with congenital central hypoventilation syndrome--mutation in PHOX2b gene and late-onset CHS.
Cyclic AMP metabolism in fragile X syndrome.
In pursuit (and discovery) of a genetic basis for congenital central hypoventilation syndrome.
Qamar, Sanaa
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In pursuit (and discovery) of a genetic basis for congenital central hypoventilation syndrome.
In pursuit (and discovery) of a genetic basis for congenital central hypoventilation syndrome. Respir Physiol Neurobiol. 2005 Nov 15; 149(1-3):73-82.
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PubMed
subject areas
Child
Child, Preschool
Homeodomain Proteins
Humans
Hypoventilation
Infant
Infant, Newborn
Mutation
Transcription Factors
authors with profiles
Elizabeth M Berry-Kravis