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History (34)
Embolic stroke due to left atrial thrombus 2 years after PFO closure.
ABC transporter polymorphisms are associated with irinotecan pharmacokinetics and neutropenia.
A genomic regulatory element that directs assembly and function of immune-specific AP-1-IRF complexes.
Pelvic congestion syndrome-associated pelvic pain: a systematic review of diagnosis and management.
Cerebellar and posterior fossa malformations in patients with autism-associated chromosome 22q13 terminal deletion.
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Cerebellar and posterior fossa malformations in patients with autism-associated chromosome 22q13 terminal deletion.
Cerebellar and posterior fossa malformations in patients with autism-associated chromosome 22q13 terminal deletion. Am J Med Genet A. 2013 Jan; 161A(1):131-6.
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PubMed
subject areas
Adaptor Proteins, Signal Transducing
Adolescent
Autistic Disorder
Cerebellum
Child
Child, Preschool
Chromosome Deletion
Chromosome Disorders
Chromosome Mapping
Chromosomes, Human, Pair 22
Developmental Disabilities
Genetic Association Studies
Genetic Loci
Genotype
Humans
Image Processing, Computer-Assisted
In Situ Hybridization, Fluorescence
Infant
Mutation
Nerve Tissue Proteins
Oligonucleotide Array Sequence Analysis
Phenotype
Polymorphism, Single Nucleotide
authors with profiles
William B. Dobyns