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Publications by Alexa T. McCray
Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome With Intellectual Disability and Developmental Delay
American Journal of Human Genetics
Genetics
IRF2BPL Is Associated With Neurological Phenotypes
American Journal of Human Genetics
Genetics
De Novo Variants in WDR37 Are Associated With Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia
American Journal of Human Genetics
Genetics
Bi-Allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes
American Journal of Human Genetics
Genetics
Modeling the Autism Spectrum Disorder Phenotype
Neuroinformatics
Neuroscience
Information Systems
Software
Characteristics of Undiagnosed Diseases Network Applicants: Implications for Referring Providers
BMC Health Services Research
Health Policy
Iterative Evaluation of a Web-Based Health Information Resource
Journal of Health Communication
Information Sciences
Communication
Public Health
Library
Environmental
Health
Occupational Health
Mapping the Gene Ontology Into the Unified Medical Language System
Comparative and Functional Genomics
An Upper-Level Ontology for the Biomedical Domain
Comparative and Functional Genomics
