Home
About
Overview
Sharing Data
ORCID
Help
History (51)
Advances in spike localization with EEG dipole modeling.
Microlissencephaly: a heterogeneous malformation of cortical development.
Patient with bilateral periventricular nodular heterotopia and polymicrogyria with apparently balanced reciprocal translocation t(1;6)(p12;p12.2) that interrupts the mannosidase alpha, class 1A, and glutathione S-transferase A2 genes.
Lissencephaly and other malformations of cortical development: 1995 update.
A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3.
See All 51 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
A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3.
A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3. Hum Mol Genet. 1997 Feb; 6(2):147-55.
View in:
PubMed
subject areas
1-Alkyl-2-acetylglycerophosphocholine Esterase
Abnormalities, Multiple
Base Sequence
Brain
Chromosomes, Human, Pair 17
Cosmids
DNA, Complementary
Face
Gene Deletion
Humans
In Situ Hybridization, Fluorescence
Microtubule-Associated Proteins
Molecular Sequence Data
Promoter Regions, Genetic
Proteins
Syndrome
authors with profiles
William B. Dobyns