Dr. Gregory Brian Peters D.D.S.
Dentist | General Practice
6180 Clay St Riverside CA, 92509About
Dr. Gregory Peters is a Dentist practicing in Riverside, CA. Dr. Peters specializes in preventing, diagnosing, and treating diseases and conditions associated with the mouth and overall dental health. Dentists are trained to carry out such treatment as professional cleaning, restorative, prosthodontic, and endodontic procedures, and performing examinations, among many others.
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Expert Publications
Data provided by the National Library of Medicine- Axenfeld-Rieger malformation and distinctive facial features: Clues to a recognizable 6p25 microdeletion syndrome.
- Chromosome microdissection identifies genomic amplifications associated with drug resistance in a leukemia cell line: an approach to understanding drug resistance in cancer.
- Paternally inherited submicroscopic duplication at 11p15.5 implicates insulin-like growth factor II in overgrowth and Wilms' tumorigenesis.
- Concurrent transposition of distal 6p and 20q to the 22q telomere: a recurrent
- Chromosomal rearrangements and novel genes in disorders of eye development, cataract and glaucoma.
- Fibrosarcomatous variant of dermatofibrosarcoma protuberans showing COL1A1-PDGFB gene fusion, detected using a novel and disease-specific RT-PCR protocol.
- Familial 7q21.3 microdeletion involving epsilon-sarcoglycan causing myoclonus dystonia, cognitive impairment, and psychosis.
- Infantile convulsions and paroxysmal kinesigenic dyskinesia with 16p11.2 microdeletion.
- Chromosome microarray in Australia: a guide for paediatricians.
- Microdeletions detected using chromosome microarray in children with suspected genetic movement disorders: a single-centre study.
- 14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett
- Challenges in identifying candidate amplification targets in human cancers: chromosome 8q21 as a case study.
- Chromosome microarrays in diagnostic testing: interpreting the genomic data.
- Deletion of protein tyrosine phosphatase, non-receptor type 4 (PTPN4) in twins with a Rett syndrome-like phenotype.
- A balanced paternal interchromosomal reciprocal insertion between 5q12.1q13.2 and 20p12.3p12.1 resulting in separate genetic conditions in two siblings.
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