Home
About
Overview
Sharing Data
ORCID
Help
History (47)
Childhood stroke and lupus anticoagulant.
Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture.
Osteoradionecrosis of the jaws as a risk factor in radiotherapy: a report of an eight-year retrospective review.
The spectrum of olfactory neural tumors. A light-microscopic immunohistochemical and ultrastructural analysis.
Lissencephaly and subcortical band heterotopia: molecular basis and diagnosis.
See All 47 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
Lissencephaly and subcortical band heterotopia: molecular basis and diagnosis.
Lissencephaly and subcortical band heterotopia: molecular basis and diagnosis. Mol Med Today. 2000 Jul; 6(7):277-84.
View in:
PubMed
subject areas
1-Alkyl-2-acetylglycerophosphocholine Esterase
Brain Diseases
Cerebral Cortex
Chromosomes, Human, Pair 17
Genetic Counseling
Humans
Microtubule-Associated Proteins
Mutation
Neuropeptides
Prenatal Diagnosis
X Chromosome
authors with profiles
William B. Dobyns