Dr. Willis Hull Murphey D.D.S.,M.S.
Orthodontist
2512 Horne St Suite A Fort Worth TX, 76107About
Dr. Willis Murphey practices Orthodontics in Fort Worth, TX. Comprehensive orthodontic treatment includes metal wires that are inserted into orthodontic brackets, which can be made from stainless steel or a more aesthetic ceramic material. The wires interact with the brackets to move teeth into desired positions. Being advanced in the field, Dr. Murphey may also use Invisalign or other aligner trays that have been designed to align a patients? smile. As an orthodontist, Dr. Murphey must recognize various characteristics of a malocclusion or dentofacial deformity, define the nature of the problem, including the etiology if possible, and design a treatment strategy based on the specific needs and desires of the patient.
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Obstructive airway disease associated with heterozygous alpha-1-antitrypsin deficiency.
- Interview: Influencing the men that I did.
- GENETIC RECOMBINATION BY TRANSDUCTION BETWEEN MANNITOL-NEGATIVE MUTANTS OF
- MANNITOL CATABOLISM BY STAPHYLOCOCCUS AUREUS.
- Molecular advances in retinitis pigmentosa.
- Neonatal screening for alpha1-antitrypsin deficiency.
- Neonatal screening for alpha1-antitrypsin deficiency.
- Screening tests for argininosuccinic aciduria, orotic aciduria, and other inherited enzyme deficiencies using dried blood specimens.
- Selective medium for carbohydrate-utilizing transductants of Staphylococcus aureus.
- Malate dehydrogenases. 3. Alteration of catalytic properties during purification of Bacillus subtilis malate dehydrogenases.
- Serum carnosinase deficiency concomitant with mental retardation.
- Oxytetracycline microfluorescent comparison of orthodontic retraction into recent and healed extraction sites.
- Studies on malate dehydrogenases and aspartate aminotransferases from Neurospora crassa.
- Malate dehydrogenases. I. A survey of molecular size measured by gel filtration.
- Erythropoietic protoporphyria, heterozygous cystinuria, and reduced peptidase A activity in a patient with 46,XX/46,XX,18q--mosaicism.
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