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PETROS TSIPOURAS, MD
MD
Clinical Cytogenetics Physician
NPI: 1699772962Individual
Specialties, Licenses & Credentials
Clinical Cytogenetics PhysicianPrimary
Medical Genetics — Clinical Cytogenetics
Code: 207SC0300X
027923(CT)
Research & Publications (20)
Gain of 3q26: a genetic marker in low-grade squamous intraepithelial lesions (LSIL) of the uterine cervix.
PMID 19394683·Gynecol Oncol·2009
8-other
Detection of circulating tumour cells in peripheral blood with an automated scanning fluorescence microscope.
PMID 18682708·Br J Cancer·2008
8-other
Detection of circulating fetal cells utilizing automated microscopy: potential for noninvasive prenatal diagnosis of chromosomal aneuploidies.
PMID 18646239·Prenat Diagn·2008
8-other
Automated microscopy of amniotic fluid cells: detection of FISH signals using the FastFISH imaging system.
PMID 16969008·Fetal Diagn Ther·2006
8-other
Endogenously expressed multimeric self-cleaving hammerhead ribozymes ablate mutant collagen in cellulo.
PMID 15963928·Mol Ther·2005
7-preclinical
Automated detection of rare fetal cells in maternal blood: eliminating the false-positive XY signals in XX pregnancies.
PMID 15284738·Am J Obstet Gynecol·2004
4-observational
Enhanced intracellular availability and survival of hammerhead ribozymes increases target ablation in a cellular model of osteogenesis imperfecta.
PMID 14566359·Gene Ther·2003
7-preclinical
Split hand foot malformation is associated with a reduced level of Dactylin gene expression.
PMID 12974740·Clin Genet·2003
4-observational
A recurring FBN1 gene mutation in neonatal Marfan syndrome.
PMID 12413333·Arch Pediatr Adolesc Med·2002
5-case
Cloning, chromosomal organization and expression analysis of Neurl, the mouse homolog of Drosophila melanogaster neuralized gene.
PMID 11997106·Biochim Biophys Acta·2002
4-observational
Delivery of a hammerhead ribozyme specifically downregulates mutant type I collagen mRNA in a murine model of osteogenesis imperfecta.
PMID 11763351·Antisense Nucleic Acid Drug Dev·2001
7-preclinical
Distal limb malformations: underlying mechanisms and clinical associations.
PMID 11595015·Clin Genet·2001
6-review
Novel approach to the molecular diagnosis of Marfan syndrome: application to sporadic cases and in prenatal diagnosis.
PMID 11251996·Am J Med Genet·2001
5-case
Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene.
PMID 11090342·Am J Hum Genet·2001
8-other
Orthopaedic manifestations of Ehlers-Danlos syndrome.
PMID 10906878·Clin Orthop Relat Res·2000
8-other
Localization of an acromesomelic dysplasia on chromosome 9 by homozygosity mapping.
PMID 10845568·Clin Genet·2000
8-other
Split-hand/split-foot malformation is caused by mutations in the p63 gene on 3q27.
PMID 10839977·Am J Hum Genet·2000
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 65 KANE ST
WEST HARTFORD, CT 06119 - Phone
- (860) 523-6464
Quick Facts
- NPI
- 1699772962
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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