Search Results - "Bernreuter, Kristen"

Deceptively benign low-grade fibromyxoid sarcoma: array-comparative genomic hybridization decodes the diagnosis by Odem, Jamie L., MD, Oroszi, Gabor, MD, Bernreuter, Kristen, BS, Grammatopoulou, Vasiliki, MS, Lauer, Scott R., MD, Greenberg, David D., MD, Vogler, Carole A., MD, Batanian, Jacqueline R., PhD

“…Summary Low-grade fibromyxoid sarcoma (previously known as Evans tumor) is a rare soft tissue neoplasm characterized by a deceptively bland appearance despite…”
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Narrowing down the common deleted region of 5q to 6.0 Mb in blastic plasmacytoid dendritic cell neoplasms by Fu, Yumei, Fesler, Mark, Mahmud, Gibran, Bernreuter, Kristen, Jia, Dongmei, Batanian, Jacqueline R

“…Abstract Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare and aggressive hematologic malignancy. Simple and complex recurrent cytogenetic…”
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Oculo-auriculo-vertebral spectrum, cat eye, and distal 22q11 microdeletion syndromes: A unique double rearrangement by Torti, Erin E., Braddock, Stephen R., Bernreuter, Kristen, Batanian, Jacqueline R.

“…An array‐CGH on 19‐year‐old male showed a proximal 1.11 Mb duplication and a distal 1.7 Mb deletion of 22q11.2 regions flanking the Velocardiofacial/DiGeorge…”
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Cryptic insertion of 3'FOXO1 into inverted chromosome arm 2q in the presence of two normal chromosome 13s and 13 small interstitial duplications in a patient with alveolar rhabdomyosarcoma by Hackman, Sarah, Calvey, Laura, Bernreuter, Kristen, Mark, Mengya Wang, Starnes, Sarah, Batanian, Jacqueline R

“…Alveolar rhabdomyosarcoma (ARMS) is a pediatric soft tissue neoplasm with a characteristic translocation, t(2;13)(q35;q14), which is detected in 70-80% of…”
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Cryptic insertion of 3′ FOXO1 into inverted chromosome arm 2q in the presence of two normal chromosome 13s and 13 small interstitial duplications in a patient with alveolar rhabdomyosarcoma by Hackman, Sarah, Calvey, Laura, Bernreuter, Kristen, Mark, Mengya Wang, Starnes, Sarah, Batanian, Jacqueline R

“…Alveolar rhabdomyosarcoma (ARMS) is a pediatric soft tissue neoplasm with a characteristic translocation, t(2;13)(q35;q14), which is detected in 70–80% of…”
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Coexistence of neocentromeric marker 3q and trisomy 3 in two different tissues in a 3-year-old boy with peripheral T-cell lymphoma: support for a gene dosage effect hypothesis by Batanian, Jacqueline R., Bernreuter, Kristen, Koslosky, Lori, Frater, John L.

“…A very small supernumerary de novo marker chromosome was ascertained during cytogenetic diagnosis of a 3½-year-old boy with peripheral T-cell lymphoma,…”
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Deletion of MYC and presence of double minutes with MYC amplification in a morphologic acute promyelocytic leukemia–like case lacking RARA rearrangement: could early exclusion of double-minute chromosomes be a prognostic factor? by Frater, John L., Hoover, Richard G., Bernreuter, Kristen, Batanian, Jacqueline R.

“…Gene amplification on double minutes is rarely found in acute myeloid leukemia (AML) and is often linked to poor prognosis. It is often associated with acute…”
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