Home
About
Overview
Sharing Data
ORCID
Help
History (4)
Assessment of Paraspinal Muscle Cross-sectional Area After Lumbar Decompression: Minimally Invasive Versus Open Approaches.
Correlation of LINE-1 Hypomethylation With Size and Pathologic Extent of Dysplasia in Colorectal Tubular Adenomas.
J.-M. Charcot and simulated neurologic disease: attitudes and diagnostic strategies.
Variable human phenotype associated with novel deletions of the PHOX2B gene.
See All 4 Pages
Find People
Find Everything
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
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.
View in:
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
Pallavi Patwari
Elizabeth Berry-Kravis