Home
About
Overview
Sharing Data
ORCID
Help
History (5)
Congenital central hypoventilation syndrome: mutation analysis of the receptor tyrosine kinase RET.
Mayahara, Masako
Mercaptoethylamines
Predescu, Dan
Species-specific alternative splicing of the epidermal growth factor-like domain 1 of cartilage aggrecan.
See All 5 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
Congenital central hypoventilation syndrome: mutation analysis of the receptor tyrosine kinase RET.
Congenital central hypoventilation syndrome: mutation analysis of the receptor tyrosine kinase RET. Am J Med Genet. 1996 Jun 28; 63(4):603-9.
View in:
PubMed
subject areas
Child
Drosophila Proteins
Humans
Hypoventilation
Karyotyping
Mutation
Polymorphism, Single-Stranded Conformational
Proto-Oncogene Proteins
Proto-Oncogene Proteins c-ret
Receptor Protein-Tyrosine Kinases
Sleep Apnea Syndromes
authors with profiles
Jean M Silvestri