the condition of lacking one member of a chromosomal pairing
monosomy (loss of one of the two chromosome 22s normally present in a cell) was foundto be associated with meningioma
Examples of 'monosomy' in a sentence
monosomy
At that time, monosomy 7 was detected by chromosomal analysis.
Yasuhiro Tanaka, Atsushi Tanaka, Akiko Hashimoto, Kumiko Hayashi, Isaku Shinzato 2017, 'Acute Myeloid Leukemia with Basophilic Differentiation Transformed from MyelodysplasticSyndrome', Case Reports in Hematologyhttp://dx.doi.org/10.1155/2017/4695491. Retrieved from DOAJ CC BY 4.0 (https://creativecommons.org/licenses/by-sa/4.0/legalcode)
Monosomy 7 and complex karyotypes were present in 44.4% and 37%, respectively.
Roberta Sandra da Silva Tanizawa, Cristina Aiko Kumeda, Raymundo Soares de AzevedoNeto, Aline de Medeiros Leal, Patrícia de Barros Ferreira, Elvira Deolinda RodriguesPereira Velloso 2011, 'Karyotypic and fluorescent in-situ hybridization study of the centromere of chromosome7 in secondary myeloid neoplasms', Revista Brasileira de Hematologia e Hemoterapiahttp://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842011000600010. Retrieved from DOAJ CC BY 4.0 (https://creativecommons.org/licenses/by-sa/4.0/legalcode)
Monosomy of chromosome 14 has been reported in only a few prenatal cases.
Javier Sánchez, Lutgardo García-Díaz, David Chinchón, Guillermo Antiñolo 2012, 'Prenatal Diagnosis of a Fetus with Congenital Heart Defect and Ring Chromosome 14',Case Reports in Geneticshttp://dx.doi.org/10.1155/2012/794075. Retrieved from DOAJ CC BY 4.0 (https://creativecommons.org/licenses/by-sa/4.0/legalcode)
Monosomy 7 was present in 18% of patients.
Özlem Tüfekçi, Ülker Koçak, Zühre Kaya, İdil Yenicesu, Canan Albayrak, Davut Albayrak,Şebnem Yılmaz Bengoa, Türkan Patıroğlu, Musa Karakükçü, Ekrem Ünal, Elif Ünal İnce,Talia İleri, Mehmet Ertem, Tiraje Celkan, Gül Nihal Özdemir, Nazan Sarper, Dilek Kaçar,Neşe Yaralı, Namık Yaşar Özbek, Alphan Küpesiz, Tuba Karapınar, Canan Vergin, ÜmranÇalışkan, Hüseyin Tokgöz, Melike Sezgin Evim, Birol Baytan, Adalet Meral Güneş, DenizYılmaz Karapınar, Serap Karaman, Vedat Uygun, Gülsun Karasu, Mehmet Akif Yeşilipek,Ahmet Koç, Erol Erduran, Berna Atabay, Haldun Öniz, Hale Ören 2018, 'Juvenile Myelomonocytic Leukemia in Turkey: A Retrospective Analysis of Sixty-fivePatients', Turkish Journal of Hematologyhttp://www.tjh.com.tr/jvi.aspx?pdir=tjh&plng=eng&un=TJH-62372. Retrieved from DOAJ CC BY 4.0 (https://creativecommons.org/licenses/by-sa/4.0/legalcode)
Conventional and molecular cytogenetic analysis revealed monosomy of chromosome 7.
Terezinha de Jesus Marques-Salles, Eliane Maria Soares-Ventura, Nathalia Lopes deOliveira, Mariluze Silva, Reijane Assis, Vera Lúcia Lins de Morais, Luize Otero, TeresaFernandez, Maria do Socorro Pombo-de-Oliveira, Maria Tereza Cartaxo Muniz, Neide Santos 2008, 'Myeloproliferative syndrome of monosomy 7: a brief report', Genetics and Molecular Biologyhttp://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572008000100007. Retrieved from DOAJ CC BY 4.0 (https://creativecommons.org/licenses/by-sa/4.0/legalcode)
Structural anomalies associated with partial 2p monosomy are rare.
Pen-Hua Su, Jia-Yuh Chen, Teng-Fu Tsao, Suh-Jen Chen 2011, 'De Novo Interstitial Deletion of Chromosome 2 (p23p24)', Pediatrics and Neonatologyhttp://www.sciencedirect.com/science/article/pii/S1875957210000094. Retrieved from DOAJ CC BY 4.0 (https://creativecommons.org/licenses/by-sa/4.0/legalcode)
Monosomy 7 was present in 35% of the patients.
Amal Al-Seraihy, Mouhab Ayas, Randa Al-Nounou, Hassan El-Solh, Ali Al-Ahmari, AbdullahAl-Jefri, Asim Belgaumi 2011, 'Outcome of allogeneic stem cell transplantation with a conditioning regimen of busulfan,cyclophosphamide and low-dose etoposide for children with myelodysplastic syndrome',Hematology/Oncology and Stem Cell Therapyhttp://www.sciencedirect.com/science/article/pii/S165838761150024X. Retrieved from DOAJ CC BY 4.0 (https://creativecommons.org/licenses/by-sa/4.0/legalcode)
Monosomy of chromosomes 8, 14, 22 or 17 was observed in three lines.
Vandana Relan, Leanne Morrison, Kylie Parsonson, Belinda E Clarke, Edwina E Duhig,Morgan N Windsor, Kevin S Matar, Rishendran Naidoo, Linda Passmore, Elizabeth McCaul,Deborah Courtney, Ian A Yang, Kwun M Fong, Rayleen V Bowman 2013, 'Phenotypes and karyotypes of human malignant mesothelioma cell lines.', PLoS ONEhttp://europepmc.org/articles/PMC3597627?pdf=render. Retrieved from PLOS CC BY 4.0 (https://creativecommons.org/licenses/by-sa/4.0/legalcode)
Four patients (8%) were identified to harbor monosomy of chromosome 3.
Masood Naseripour, Mitra Mehrazma, Rama Pourmatin, Mohsen Bahmani Kashkouli, AhadSedaghat, Elmira Gheytanchi 2015, 'Monosomy 3 by chromogenic in situ hybridization (CISH) in Iranian patients with uvealmelanoma', Journal of Current Ophthalmologyhttp://www.sciencedirect.com/science/article/pii/S2452232515000037. Retrieved from DOAJ CC BY 4.0 (https://creativecommons.org/licenses/by-sa/4.0/legalcode)