Showing 161 - 180 results of 260 for search '"cytogenetics"', query time: 0.05s Refine Results
  1. 161

    Ovarian Fetiform Teratoma in 38 Years Nulliparous Woman: A Case Report by Desalew Gedamu, Mekitie Wondafrash, Meron Berhanu

    Published 2025-01-01
    “…To establish the diagnosis, a thorough clinicopathologic examination, laboratory tests for pregnancy and relevant cytogenetic tests for Zygosity should be performed.…”
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    Article
  2. 162

    Novel Vascular Malformation in an Affected Newborn with Deletion Del(4)(q31.3) by Norma Elena de León Ojeda, Michel Soriano-Torres, Mercedes J. Cabrera, Dunia Bárbara Benítez Ramos

    Published 2012-01-01
    “…The parents were cytogenetically normal. We compare clinical signs to other cases with a deletion in long arm of chromosome 4.…”
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    Article
  3. 163

    Vertigo as the First Sign of Chronic Myeloid Leukemia: A Case Report and Literature Review by Rubén Martín-Hernández, Diego Hernando Macías-Rodríguez, Víctor Martín-Sánchez, Cristina Cordero-Civantos, Santiago Santa Cruz-Ruiz, Ángel Batuecas-Caletrio

    Published 2013-01-01
    “…A peripheral blood cytogenetic analysis is performed due to a high suspicion of leukemia, and the results show BCR/ABL fusion gene with a cut point in the M-BCR region, which confirms the diagnosis of chronic myeloid leukemia. …”
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    Article
  4. 164

    Durable Leukemic Remission and Autologous Marrow Recovery with Random Chromosomal Abnormalities after Allogeneic Hematopoietic Stem Cell Transplantation for Chronic Lymphocytic Leu... by Hidekazu Nishikii, Naoki Kurita, Atsushi Shinagawa, Tatsuhiro Sakamoto, Manabu Kusakabe, Yasuhisa Yokoyama, Takayasu Kato, Mamiko Sakata-Yanagimoto, Naoshi Obara, Yuichi Hasegawa, Naoya Nakamura, Shigeru Chiba

    Published 2019-01-01
    “…Nevertheless, B-cell clonality became undetectable at 14 days after transplant, which has been kept so for over 10 years with clinical remission. Cytogenetic analyses were repeatedly performed and demonstrated nonclonal chromosomal aberrations, although the patient did not develop any secondary malignancies. …”
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    Article
  5. 165

    Primary Synovial Sarcoma of the Scrotum by Nourah Al-Oudah, Sara Alanazi, Sarah Saad Alotaibi, Nayef Alzahrani

    Published 2023-01-01
    “…The tumor stained positive for pancytokeratin, AE1/AE3, epithelial membrane antigen (EMA), TLE-1, CD99, and BCL-2. The cytogenetic testing showed a chromosomal translocation in the SS18 gene at 18q11.2, consistent with the diagnosis of primary synovial sarcoma. …”
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    Article
  6. 166

    Tumor venéreo transmissível canino com resistência quimioterápica e metástase esplênica. Relato de caso by A. P. Duzanski, A. D. Ortiz, H. B. Fêo, M. W. Fonseca, M. M. Flórez, L. T Rodrigues, F. Michelon, N. S. Rocha

    Published 2019-01-01
    “…After the cytological, histological and cytogenetic diagnostic, the primary tumor was still characterized in progression phase and showed low major histocompatibility complex expression MHC (4,4 ± 2% class I e 11 ± 4,1% class II. …”
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    Article
  7. 167

    Molecular Profiling: A Case of ZBTB16-RARA Acute Promyelocytic Leukemia by Stephen E. Langabeer, Lisa Preston, Johanna Kelly, Matt Goodyer, Ezzat Elhassadi, Amjad Hayat

    Published 2017-01-01
    “…The clinical course together with the cytogenetic and molecular characterization of a case of ATRA-unresponsive ZBTB16-RARA APL is described. …”
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    Article
  8. 168

    A Multidisciplinary Approach to the Management of Atypical Osseous Epithelioid Hemangioendothelioma by J. K. Ma, J. Barr, S. Vijayakumar

    Published 2014-01-01
    “…Herein, the authors discuss the imaging characteristics, histopathological aspects, cytogenetic findings, and the radiobiological behavior of osseous EH. …”
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    Article
  9. 169

    Chronic Eosinophilic Leukemia Presenting as Cardiac Failure by Nii Boi-Doku Pepra-Ameyaw, William Kwasi Ghunney, Eugene Baafi Ampofo, Edeghonghon Olayemi

    Published 2022-01-01
    “…Good symptomatic control was achieved using hydroxyurea after which haematologic and cytogenetic remission was achieved after 12 weeks on a tyrosine kinase inhibitor. …”
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    Article
  10. 170

    An Interstitial 4q Deletion with a Mosaic Complementary Ring Chromosome in a Child with Dysmorphism, Linear Skin Pigmentation, and Hepatomegaly by J. Carter, H. Brittain, D. Morrogh, N. Lench, J. J. Waters

    Published 2017-01-01
    “…This case highlights the importance of an integrated approach to cytogenetic analysis and demonstrates the value of G-banding for detecting mosaicism, as current microarray platforms are unable to detect low level mosaics.…”
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    Article
  11. 171

    Congenital Absence of a Teat in a Japanese Black Heifer by Mohamed Elshabrawy Ghanem, Toshihiko Nakao, Chikako Yoshida

    Published 2011-01-01
    “…Blood samples were taken for cytogenetic and DNA testing. The heifer had normal chromosomal set. …”
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    Article
  12. 172

    Adult acute megakaryoblastic leukemia with persistent diarrhea and extreme thrombocytosis: A very unusual case by Nevin Alayvaz Aslan, Gülsün Gülten

    Published 2024-04-01
    “…The hematologic evaluation included peripheral blood smear, bone marrow aspiration and biopsy, flow cytometry, and cytogenetic analysis. Eventually, according to pathologic and flow cytometric findings, a diagnosis of AML-M7 was made. …”
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    Article
  13. 173
  14. 174

    In-depth inference of transcriptional regulatory networks reveals NPM1 as a therapeutic ribosomal regulator in MYC-amplified medulloblastoma by Tong Chen, Huiyao Chen, Mingyang Xia, Yunfei Liao, Hao Li, Xinran Dong, Yifeng Lin, Wenhao Zhou

    Published 2025-01-01
    “…Identifying subtype-specific signatures within Group 3 and Group 4 remains challenging due to shared cytogenetic alterations and limitations of conventional differential gene expression analysis. …”
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    Article
  15. 175

    Flow Cytometric DNA Index and Karyotype in Childhood Lymphoblastic Leukemia by Erik Forestier, Gösta Holmgren, Göran Roos

    Published 1998-01-01
    “…During treatment aneuploid clones could be detected by DIFCM in a substantial number of cases where the cytogenetic analysis was normal, and the opposite was also demonstrated in one case. …”
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  16. 176

    SHOX Duplication and Tall Stature in a Patient with Xq Deletion and Vascular Disease by J. M. Ramirez, F. A. Rodríguez, M. I. Echeverría, A. L. Vargas, A. E. Calderón, R. M. Miatello, N. F. Renna

    Published 2019-01-01
    “…We have proposed that cytogenetic anomalies in X chromosome could contribute to decrease this protein synthesis in this gender.…”
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    Article
  17. 177

    A Rare 46,X,t(Y;10)(q12;p14) Balanced Translocation in Non-Obstructive Azoospermic Patient with Elevated FSH and LH Levels by Kousar Jahan Syeeda Khursheed, Mohammed Rahman Kaleemullah, Annu Joseph, Mohammed Hasan Al Durazi, Moiz Bakhiet

    Published 2023-01-01
    “…Thus, our study points to the importance of conventional cytogenetic techniques in the preliminary evaluation of a genetic abnormality in cases of infertility and would help the patient make an informed decision before pursuing assisted reproductive technology.…”
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    Article
  18. 178

    Te fauna of mosquitoes (Diptera: Culicidae) of Armenia by V.A. Burlak, Yu.V. Andreeva, O.V. Shcherbakov, V.S. Fedorova, E.S. Soboleva, M.K. Haidara, S.S. Alekseeva, R.V. Slobodyanik, H.S. Gevorgyan, S.A. Aghayan, G.N. Artemov

    Published 2025-01-01
    “…In addition to using cytogenetic and molecular diagnostic methods, the larvae and adults morphological characteristics or egg chorion pattern were used to identify 1607 adults and 392 larvae. …”
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    Article
  19. 179

    A Turner Syndrome Patient Carrying a Mosaic Distal X Chromosome Marker by Roberto L. P. Mazzaschi, Juliet Taylor, Stephen P. Robertson, Donald R. Love, Alice M. George

    Published 2014-01-01
    “…This case report has a phenotype that is largely discordant with previously published cases as it lies at the severe end of the Turner variant phenotype scale. The observed cytogenetic abnormalities in this study may represent a coincidental finding, but we cannot exclude the possibility that the marker has a nonfunctioning X chromosome inactivation locus, leading to functional disomy of those genes carried by the marker.…”
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    Article
  20. 180

    Rat Sarcoma Virus Family Genes in Acute Myeloid Leukemia: Pathogenetic and Clinical Implications by Shaimaa Khattab, Adriatik Berisha, Natalia Baran, Pier Paolo Piccaluga

    Published 2025-01-01
    “…Despite using molecular and cytogenetic risk classification to guide treatment decisions, most AML patients survive for less than five years. …”
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    Article