 Monosomy
"Monosomy" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
The condition in which one chromosome of a pair is missing. In a normally diploid cell it is represented symbolically as 2N-1.
| Descriptor ID |
D009006
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| MeSH Number(s) |
C23.550.210.050.500 G05.365.590.175.050.500 G05.700.131.500
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Monosomy".
Below are MeSH descriptors whose meaning is more specific than "Monosomy".
This graph shows the total number of publications written about "Monosomy" by people in this website by year, and whether "Monosomy" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 1 | 0 | 1 | | 1999 | 0 | 1 | 1 | | 2003 | 1 | 0 | 1 | | 2004 | 1 | 0 | 1 | | 2010 | 1 | 1 | 2 | | 2014 | 0 | 1 | 1 | | 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Monosomy" by people in Profiles.
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Guzewicz L, Howell S, Crerand CE, Umbaugh H, Nokoff NJ, Barker J, Davis SM. Clinical phenotype and management of individuals with mosaic monosomy X with Y chromosome material stratified by genital phenotype. Am J Med Genet A. 2021 05; 185(5):1437-1447.
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Liu Y, Liu Y, Chen H, Li Q, Meng L, Chen L, Du T, Zhang J. Relationship of karyotype to embryo crown-rump length and maternal serum human chorionic gonadotropin level in early miscarriage. Am J Perinatol. 2015 Jan; 32(1):15-22.
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Gajecka M, Saitta SC, Gentles AJ, Campbell L, Ciprero K, Geiger E, Catherwood A, Rosenfeld JA, Shaikh T, Shaffer LG. Recurrent interstitial 1p36 deletions: Evidence for germline mosaicism and complex rearrangement breakpoints. Am J Med Genet A. 2010 Dec; 152A(12):3074-83.
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Kleinschmidt-DeMasters BK, Alassiri AH, Birks DK, Newell KL, Moore W, Lillehei KO. Epithelioid versus rhabdoid glioblastomas are distinguished by monosomy 22 and immunohistochemical expression of INI-1 but not claudin 6. Am J Surg Pathol. 2010 Mar; 34(3):341-54.
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Trobaugh-Lotrario AD, Kletzel M, Quinones RR, McGavran L, Proytcheva MA, Hunger SP, Malcolm J, Schissel D, Hild E, Giller RH. Monosomy 7 associated with pediatric acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS): successful management by allogeneic hematopoietic stem cell transplant (HSCT). Bone Marrow Transplant. 2005 Jan; 35(2):143-9.
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Mumtaz MA, Mee RB, Qureshi A, Patel CR, Younoszai AK. HLHS with severe aortic insufficiency in a patient with 45,X/46,XY mosaicism. Ann Thorac Surg. 2004 Oct; 78(4):1475-6.
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Kesler SR, Garrett A, Bender B, Yankowitz J, Zeng SM, Reiss AL. Amygdala and hippocampal volumes in Turner syndrome: a high-resolution MRI study of X-monosomy. Neuropsychologia. 2004; 42(14):1971-8.
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Kesler SR, Blasey CM, Brown WE, Yankowitz J, Zeng SM, Bender BG, Reiss AL. Effects of X-monosomy and X-linked imprinting on superior temporal gyrus morphology in Turner syndrome. Biol Psychiatry. 2003 Sep 15; 54(6):636-46.
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Luna-Fineman S, Shannon KM, Atwater SK, Davis J, Masterson M, Ortega J, Sanders J, Steinherz P, Weinberg V, Lange BJ. Myelodysplastic and myeloproliferative disorders of childhood: a study of 167 patients. Blood. 1999 Jan 15; 93(2):459-66.
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Luna-Fineman S, Shannon KM, Lange BJ. Childhood monosomy 7: epidemiology, biology, and mechanistic implications. Blood. 1995 Apr 15; 85(8):1985-99.
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