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MATTHEW SPEICHER, M.D.
M.D.
Internal Medicine Physician
NPI: 1629086020Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
ME24150(FL)
Research & Publications (20)
Predictive diagnosis of the cancer prone Li-Fraumeni syndrome by accident: new challenges through whole genome array testing.
PMID 19269943·J Med Genet·2009
5-case
Comprehensive screening for Lynch syndrome: who can be the driving force in daily clinical practice?
PMID 19307489·J Clin Oncol·2009
8-other
Humanized large-scale expanded endothelial colony-forming cells function in vitro and in vivo.
PMID 19321860·Blood·2009
7-preclinical
Identification of small gains and losses in single cells after whole genome amplification on tiling oligo arrays.
PMID 19541849·Nucleic Acids Res·2009
8-other
Clinical optical coherence tomography combined with multiphoton tomography of patients with skin diseases.
PMID 19598177·J Biophotonics·2009
3-trial
9p21 deletion in primary cutaneous large B-cell lymphoma, leg type, may escape detection by standard FISH assays.
PMID 18704105·J Invest Dermatol·2009
5-case
Persistence of DNA threads in human anaphase cells suggests late completion of sister chromatid decatenation.
PMID 17989990·Chromosoma·2008
8-other
Two novel mutations in the GDAP1 and PRX genes in early onset Charcot-Marie-Tooth syndrome.
PMID 18504680·Neuropediatrics·2008
8-other
[Precancerous lesions of the urothelium. From Feulgen staining to single cell CGH].
PMID 18604536·Pathologe·2008
8-other
Single-cell isolation from cell suspensions and whole genome amplification from single cells to provide templates for CGH analysis.
PMID 18079717·Nat Protoc·2007
8-other
Impact of array comparative genomic hybridization-derived information on genetic counseling demonstrated by prenatal diagnosis of the TAR (thrombocytopenia-absent-radius) syndrome-associated microdeletion 1q21.1.
PMID 17847015·Am J Hum Genet·2007
8-other
[Genetic counseling in multiple pregnancies].
PMID 17272932·Gynakol Geburtshilfliche Rundsch·2007
8-other
Digital karyotyping reveals frequent inactivation of the dystrophin/DMD gene in malignant melanoma.
PMID 17314512·Cell Cycle·2007
4-observational
Radial chromatin positioning is shaped by local gene density, not by gene expression.
PMID 17333233·Chromosoma·2007
8-other
Hybridize and personalize: the new age of syndromal mental retardation diagnostics.
PMID 17339578·Neurology·2007
8-other
Retroviral insertional mutagenesis identifies RUNX genes involved in chronic myeloid leukemia disease persistence under imatinib treatment.
PMID 17360569·Proc Natl Acad Sci U S A·2007
7-preclinical
Multiplex-fluorescence in situ hybridization for chromosome karyotyping.
PMID 17406400·Nat Protoc·2006
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2150 SE SALERNO RD, STE 200
STUART, FL 34997 - Phone
- (772) 223-5757
Quick Facts
- NPI
- 1629086020
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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