Home
About
Overview
Sharing Data
ORCID
Help
History (18)
Slow integration leads to persistent action potential firing in distal axons of coupled interneurons.
In vitro stimulation with WT1 peptide-loaded Epstein-Barr virus-positive B cells elicits high frequencies of WT1 peptide-specific T cells with in vitro and in vivo tumoricidal activity.
Two truncating variants in FANCC and breast cancer risk.
Advances in asthma and allergic disease genetics: Is bigger always better?
MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis.
See All 18 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
MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis.
MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis. Brain. 2020 01 01; 143(1):55-68.
View in:
PubMed
subject areas
Abnormalities, Multiple
Adolescent
Basilar Artery
Carotid Arteries
Cerebellar Vermis
Cerebellum
Child
Child, Preschool
Cohort Studies
Comparative Genomic Hybridization
Craniofacial Abnormalities
Female
Fibroblasts
Humans
Imaging, Three-Dimensional
Infant
Intellectual Disability
Language Development Disorders
Magnetic Resonance Imaging
Male
Middle Aged
Mutation
Nervous System Malformations
Nonsense Mediated mRNA Decay
Polymicrogyria
Real-Time Polymerase Chain Reaction
Syndrome
Tomography, X-Ray Computed
Trans-Activators
Tumor Suppressor Proteins
Whole Genome Sequencing
authors with profiles
Russell R. Reid
William B. Dobyns