Dr. Robert S. Wildin MD
Geneticist | Clinical Genetics (M.D.)
111 COLCHESTER AVE BURLINGTON VT, 05401About
Dr. Robert Wildin practices Genetic Medicine in Boise, ID. As a geneticist, Dr. Wildin performs experiments and analyzes data to interpret the inheritance of different traits in patients. A geneticist evaluates, diagnoses, and manages patients with hereditary conditions or congenital malformations, genetic risk calculations, and mutation analysis. Dr. Wildin carries out studies, tests, and counsels patients with genetic diseases.
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Clinical utility of direct mutation testing for congenital nephrogenic diabetes
- X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy.
- Neonatal diabetes mellitus, enteropathy, thrombocytopenia, and endocrinopathy: Further evidence for an X-linked lethal syndrome.
- Rescue of the autoimmune scurfy mouse by partial bone marrow transplantation or by injection with T-enriched splenocytes.
- Prospective immunological profiling in a case of immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX).
- IPEX and FOXP3: clinical and research perspectives.
- Identifying candidate genes for 2p15p16.1 microdeletion syndrome using clinical, genomic, and functional analysis.
- Human thyroxine-binding globulin (TBG): heterogeneity within individuals and among individuals demonstrated by isoelectric focusing.
- Functional dissection of the murine lck distal promoter.
- Heterogeneous AVPR2 gene mutations in congenital nephrogenic diabetes insipidus.
- Correlation of linkage data with phenotype in eight families with Stickler syndrome.
- AVPR2 variants and V2 vasopressin receptor function in nephrogenic diabetes insipidus.
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