Dr. Matthew R Speicher M.D.
Internist
2150 Se Salerno Rd Suite 200 Stuart FL, 34997About
Dr. Matthew Speicher is an internist practicing in Stuart, FL. Dr. Speicher specializes in the medical treatment of adults. Internists can act as a primary physician or a consultant to a primary physician. They manage both common and rare diseases. Dr. Speicher provides comprehensive care and manages treatment with surgeons as well. Internists establish long-term relationships with their patients and incorporate disease prevention and mental health care into their practice.
Education and Training
Georgetown Univ Sch of Med, Washington Dc 1970
Board Certification
Internal MedicineAmerican Board of Internal MedicineABIM
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Comparative genomic hybridization, loss of heterozygosity, and DNA sequence analysis of single cells.
- Frequent chromosomal DNA unbalance in thyroid oncocytic (Hürthle cell) neoplasms detected by comparative genomic hybridization.
- Assignment of the gene encoding mannan-binding lectin-associated serine protease 2 (MASP2) to human chromosome 1p36.3-->p36.2 by in situ hybridization and somatic cell hybrid analysis.
- A complete set of repeat-depleted, PCR-amplifiable, human chromosome-specific painting probes.
- Multiplex-FISH for pre- and postnatal diagnostic applications.
- Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3).
- An optimized probe set for the detection of small interchromosomal aberrations by use of 24-color FISH.
- Breakpoint within the nucleolus organizer region resulting in a reciprocal translocation t (4;14)(q21;p12).
- Analysis of chromosomal alterations in non-small cell lung cancer by multiplex-FISH, comparative genomic hybridization, and multicolor bar coding.
- Classification accuracy in multiple color fluorescence imaging microscopy.
- Risk estimates for carriers of chromosome reciprocal translocation t(4;9)(p15.2;p13).
- Assignment of CD163B, the gene encoding M160, a novel scavenger receptor, to human chromosome 12p13.3 by in situ hybridization and somatic cell hybrid analysis.
- Malignant potential and cytogenetic characteristics of occult disseminated tumor cells in esophageal cancer.
- Mosaicism for a dup(12)(q22q13) in a patient with hypomelanosis of Ito and asymmetry.
- Subtelomeric chromosome rearrangements are detected using an innovative 12-color FISH assay (M-TEL).
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