Medical Genetics
Dr. Philip N. Mowrey, PHD
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Philip Mowrey practices Medical Genetics. Philip Mowrey is a published doctor. He published 26 publications, including: '46,XX, inv(6)(p21.1p23) in a pedigree with hereditary haemochromatosis.'
Publications
- A novel t(10;12)(q21;p13) involving ETV6 in a patient with acute myeloid leukemia.
- Deletion 6p as the sole chromosome abnormality in a patient with therapy-related myelodysplastic syndrome: case report and review of the literature.
- A rare finding of deletion 5q in a child with juvenile myelomonocytic leukemia.
- Insertion (12;9)(p13;q34q34): a cryptic rearrangement involving ABL1/ETV6 fusion in a patient with Philadelphia-negative chronic myeloid leukemia.
- Translocation (2;8)(q35;q13): a recurrent abnormality in congenital embryonal rhabdomyosarcoma.
- Long-term persistence of nonpathogenic clonal chromosome abnormalities in donor hematopoietic cells after allogeneic stem cell transplantation.
- A case of lipoblastoma with seven copies of chromosome 8.
- 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 le...
- Dicentric (17;20)(p11.2;q11.2): an uncommon cytogenetic abnormality in myeloid malignancies.
- Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study.
- Isolated del(14)(q21) in a case of precursor B-cell acute lymphoblastic leukemia.
- Variant acute promyelocytic leukemia translocation (15;17) originating from two subsequent balanced translocations involving the same chromosomes 15 and 17 while prese...
- Unexpected retention and concomitant loss of subtelomeric regions in balanced chromosome anomalies by FISH.
- Rapid interphase analysis for prenatal diagnosis of translocation carriers using subtelomeric probes.
- Molecularly defined interstitial tandem duplication 6p case with mild manifestations.
- 46,XX, inv(6)(p21.1p23) in a pedigree with hereditary haemochromatosis.
- Should the 3C (craniocerebellocardiac) syndrome be included in the spectrum of velocardiofacial syndrome and DiGeorge sequence?
- Clinical and molecular analyses of deletion 3p25-pter syndrome.
- Malformations in a child with dup (7pter-p15.1) and del (7q36-qter) as a result of familial pericentric inversion.
- Five children with del (2)(q31q33) and one individual with dup (2)(q31q33) from a single family: review of brain, cardiac, and limb malformations.
- Neurologic manifestations in 18q- syndrome.
- Increased frequency of lymphocytic mitotic non-disjunction in recurrent spontaneous aborters.
- Interstitial del(13q) associated with blindness and mental retardation.
- Origin of nondisjunction in trisomy 21 syndrome: all studies compiled, parental age analysis, and international comparisons.
- Dissociation of a t(12;21) resulting in a normal cell line in two trisomic 21 sons of a nonmosaic t(12;21) father?
Doctors Specialties
- Clinical Cytogenetics
- Medical Genetics
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