Dr. Philip N Mowrey PH.D., M.S.
Geneticist | Clinical Cytogenetic
14225 Newbrook Dr Pob 10841 Chantilly VA, 20151About
Dr. Philip Mowrey practices Genetic Medicine in Chantilly, VA. As a geneticist, Dr. Mowrey performs experiments and analyzes data to interpret the inheritance of different traits in patients. A geneticist evaluates, diagnoses, and manages patients? with hereditary conditions or congenital malformations, genetic risk calculations, and mutation analysis. Dr. Mowrey carries out studies, tests, and counsels patients with genetic diseases.
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Isolated del(14)(q21) in a case of precursor B-cell acute lymphoblastic leukemia.
- 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.
- A case of lipoblastoma with seven copies of chromosome 8.
- Deletion 6p as the sole chromosome abnormality in a patient with therapy-related myelodysplastic syndrome: case report and review of the literature.
- A novel t(10;12)(q21;p13) involving ETV6 in a patient with acute myeloid leukemia.
- Incidence and patterns of ALK FISH abnormalities seen in a large unselected series of lung carcinomas.
- Increased frequency of lymphocytic mitotic non-disjunction in recurrent spontaneous aborters.
- Origin of nondisjunction in trisomy 21 syndrome: all studies compiled, parental age analysis, and international comparisons.
- Interstitial del(13q) associated with blindness and mental retardation.
- 46,XX, inv(6)(p21.1p23) in a pedigree with hereditary haemochromatosis.
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