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PHILIP MOWREY, PH.D., M.S.
PH.D., M.S.
Clinical Cytogenetics Physician
NPI: 1598717654Individual
Specialties, Licenses & Credentials
Clinical Cytogenetics PhysicianPrimary
Medical Genetics — Clinical Cytogenetics
Code: 207SC0300X
MOWRP1(NY)
Research & Publications (12)
Insertion (12;9)(p13;q34q34): a cryptic rearrangement involving ABL1/ETV6 fusion in a patient with Philadelphia-negative chronic myeloid leukemia.
PMID 19480935·Cancer Genet Cytogenet·2009
5-case
Translocation (2;8)(q35;q13): a recurrent abnormality in congenital embryonal rhabdomyosarcoma.
PMID 19389508·Cancer Genet Cytogenet·2009
5-case
Long-term persistence of nonpathogenic clonal chromosome abnormalities in donor hematopoietic cells after allogeneic stem cell transplantation.
PMID 19380032·Cancer Genet Cytogenet·2009
5-case
A case of lipoblastoma with seven copies of chromosome 8.
PMID 19264235·Cancer Genet Cytogenet·2009
5-case
Cryptic ins(4;11)(q21;q23q23) detected by fluorescence in situ hybridization: a variant of t(4;11)(q21;q23) in an infant with a precursor B-cell acute lymphoblastic leukemia report of a second case.
PMID 17452260·Cancer Genet Cytogenet·2007
5-case
Dicentric (17;20)(p11.2;q11.2): an uncommon cytogenetic abnormality in myeloid malignancies.
PMID 16965957·Cancer Genet Cytogenet·2006
5-case
Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study.
PMID 16882740·J Med Genet·2006
8-other
Isolated del(14)(q21) in a case of precursor B-cell acute lymphoblastic leukemia.
PMID 16080963·Cancer Genet Cytogenet·2005
5-case
Variant acute promyelocytic leukemia translocation (15;17) originating from two subsequent balanced translocations involving the same chromosomes 15 and 17 while preserving the PML/RARA fusion.
PMID 16080960·Cancer Genet Cytogenet·2005
5-case
Unexpected retention and concomitant loss of subtelomeric regions in balanced chromosome anomalies by FISH.
PMID 12124733·Am J Med Genet·2002
5-case
Rapid interphase analysis for prenatal diagnosis of translocation carriers using subtelomeric probes.
PMID 11920892·Prenat Diagn·2002
5-case
Molecularly defined interstitial tandem duplication 6p case with mild manifestations.
PMID 11746013·Am J Med Genet·2001
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 14225 NEWBROOK DR, POB 10841
CHANTILLY, VA 20151 - Phone
- (703) 802-7094
Quick Facts
- NPI
- 1598717654
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 12
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