Dr. Darrell Faubert Barker M.D.
General Practitioner
300 Hospital Rd Ddeamc Augusta GA, 30905About
Dr. Darrell Barker is a general practitioner practicing in Augusta, GA. Dr. Barker does not specialize in one area of medicine, however provides routine health care services. General practitioners typically have regular, even life-long patients who they provide health care services to. Dr. Barker provides services including physical exams, immunizations, and diagnosing and treating multiple illnesses and injuries. General practitioners typically work in private offices and clinics and have staffs of nurses and administators.
Education and Training
State University of New York / Health Science Center At Stony Brook 2005
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Evidence for effective suppression of recombination in the chromosome 17q21 segment spanning RNU2-BRCA1.
- Direct genomic multiplex PCR for BRCA1 and application to mutation detection by single-strand conformation and heteroduplex analysis.
- Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes.
- Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome?
- A CA-dinucleotide polymorphism at the D17S113 locus, which is closely linked to D17S74.
- Two CA-dinucleotide polymorphisms at the COL4A5 (Alport syndrome) gene in Xq22.
- Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease type 1).
- MRX8: an X-linked mental retardation condition with linkage to Xq21.
- Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosome.
- Localization of the highly polymorphic microsatellite DXS456 on the genetic linkage map of the human X chromosome.
- The duplication in Charcot-Marie-Tooth disease type 1a spans at least 1100 kb on chromosome 17p11.2.
- Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a). The HMSN Collaborative Research Group.
- Molecular analysis of a patient with neurofibromatosis 1 and achondroplasia.
- Two polymorphisms of the FOS oncogene.
- Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markers.
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