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DEREK VAN DYKE, D.M.D.
D.M.D.
General Practice Dentistry
NPI: 1558700666Individual
Specialties, Licenses & Credentials
General Practice DentistryPrimary
Dentist — General Practice
Code: 1223G0001X
30-024005(OH)
Research & Publications (20)
Conventional cytogenetics in myelofibrosis: literature review and discussion.
PMID 19141119·Eur J Haematol·2009
6-review
Validation of a new three-color fluorescence in situ hybridization (FISH) method to detect CHIC2 deletion, FIP1L1/PDGFRA fusion and PDGFRA translocations.
PMID 19118897·Leuk Res·2009
4-observational
Circulating blasts or myeloid precursor cells in peripheral blood can predict success of cytogenetic analysis.
PMID 19128830·Leuk Res·2009
8-other
Karyotype complements the International Prognostic Scoring System for primary myelofibrosis.
PMID 19215287·Eur J Haematol·2009
8-other
Identification of sex chromosome mosaicism: is analysis of 20 metaphase cells sufficient?
PMID 19161142·Am J Med Genet A·2009
8-other
De novo deletion 17p13.1 chronic lymphocytic leukemia shows significant clinical heterogeneity: the M. D. Anderson and Mayo Clinic experience.
PMID 19414856·Blood·2009
4-observational
Isolated trisomy 15: a clonal chromosome abnormality in bone marrow with doubtful hematologic significance.
PMID 18285273·Am J Clin Pathol·2008
8-other
Feeding and swallowing dysfunction in genetic syndromes.
PMID 18646013·Dev Disabil Res Rev·2008
6-review
Peripheral blood cytogenetic studies in myelofibrosis: overall yield and comparison with bone marrow cytogenetic studies.
PMID 18241918·Leuk Res·2008
4-observational
Peripheral blood cytogenetic studies in hematological neoplasms: predictors of obtaining metaphases for analysis.
PMID 18088399·Eur J Haematol·2008
8-other
Mosaic variegated aneuploidy without microcephaly: implications for cytogenetic diagnosis.
PMID 17632782·Am J Med Genet A·2007
5-case
Myxoinflammatory fibroblastic sarcoma showing t(2;6)(q31;p21.3) as a sole cytogenetic abnormality.
PMID 17854670·Cancer Genet Cytogenet·2007
5-case
Isochromosome (X)(p10) in hematologic disorders: FISH study of 14 new cases show three types of centromere signal patterns.
PMID 17981211·Cancer Genet Cytogenet·2007
8-other
The impact of maternal serum screening programs for Down syndrome in southeast Michigan, 1988-2003.
PMID 17546696·Prenat Diagn·2007
8-other
Microarray comparative genomic hybridization and FISH studies of an unbalanced cryptic telomeric 2p deletion/16q duplication in a patient with mental retardation and behavioral problems.
PMID 17345620·Am J Med Genet A·2007
4-observational
Methylprednisolone-rituximab is an effective salvage therapy for patients with relapsed chronic lymphocytic leukemia including those with unfavorable cytogenetic features.
PMID 18067017·Leuk Lymphoma·2007
8-other
Loss of TP53 is due to rearrangements involving chromosome region 17p10 approximately p12 in chronic lymphocytic leukemia.
PMID 16737921·Cancer Genet Cytogenet·2006
8-other
A case of mosaic supernumerary ring chromosome 15 with two copies of the segment 15p11.1-q14.
PMID 16830338·Am J Med Genet A·2006
5-case
Mosaic ring 20 with no detectable deletion by FISH analysis: Characteristic seizure disorder and literature review.
PMID 16835934·Am J Med Genet A·2006
5-case
Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study.
PMID 16882740·J Med Genet·2006
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
- 1190 INDEPENDENCE AVE
MARION, OH 43302 - Phone
- (740) 382-5535
Quick Facts
- NPI
- 1558700666
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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