Mrs. Alicia Marlane Capps PA-C
Physician Assistant
3551 ROGER BROOKE DR SAN ANTONIO TX, 78234About
Alicia Capps is a physician assistant practicing in SAN ANTONIO, TX. Alicia specializes in preventing and treating human illness and injury by providing a broad range of care under the supervision of a physician. A physician assistant's work can include physical exams, ordering and interpreting tests, performing procedures and prescribing medication. Often times, they can assist in surgery but the scope of practice can vary according to jurisdiction or health care setting.
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Expert Publications
Data provided by the National Library of Medicine- No evidence for linkage between schizophrenia and markers at chromosome 15q13-14.
- Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21.
- The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutations.
- Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III.
- Genetic heterogeneity in schizophrenia: stratification of genome scan data using co-segregating related phenotypes.
- Trisomy 12 mosaicism confirmed in multiple organs from a liveborn child.
- An apparently dominant bipolar affective disorder (BPAD) locus on chromosome 20p11.2-q11.2 in a large Turkish pedigree.
- A balanced complex chromosomal rearrangement (BCCR) in a family with reproductive failure.
- New chromosome 21 DNA markers isolated by pulsed field gel electrophoresis from an ETS2-containing Down syndrome chromosomal region.
- [The contribution of molecular genetics to clinical cardiology: the example of hypertrophic cardiomyopathy].
- Gene-dosage mapping of 30 DNA markers on chromosome 21.
- Cytogenetic and molecular analysis of a de novo tandem duplication of chromosome 21.
- Neuronal-specific expression of human copper-zinc superoxide dismutase gene in transgenic mice: animal model of gene dosage effects in Down's syndrome.
- Expression of human Cu-Zn superoxide dismutase gene in transgenic mice: model for gene dosage effect in Down syndrome.
- Experience of a multidisciplinary task force with exome sequencing for Mendelian disorders.
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