Difference between revisions of "Isochromosome 12p"
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[[Image: Isochromosome.gif |thumb|Schematic description of an isochromosome (Kazulanth/WC).]] | [[Image: Isochromosome.gif |thumb|Schematic description of an isochromosome (Kazulanth/WC).]] | ||
'''Isochromosome 12p''', abbreviated i(12p), a genetic abnormality associated with [[germ cell tumours]].<ref>{{cite journal |authors=Freitag CE, Sukov WR, Bryce AH, Berg JV, Vanderbilt CM, Shen W, Smadbeck JB, Greipp PT, Ketterling RP, Jenkins RB, Herrera-Hernandez L, Costello BA, Thompson RH, Boorjian SA, Leibovich BC, Jimenez RE, Murphy SJ, Vasmatzis G, Cheville JC, Gupta S |title=Assessment of isochromosome 12p and 12p abnormalities in germ cell tumors using fluorescence in situ hybridization, single-nucleotide polymorphism arrays, and next-generation sequencing/mate-pair sequencing |journal=Hum Pathol |volume=112 |issue= |pages=20–34 |date=June 2021 |pmid=33798590 |doi=10.1016/j.humpath.2021.03.008 |url=}}</ref> | '''Isochromosome 12p''', abbreviated '''i(12p)''', a genetic abnormality associated with [[germ cell tumours]].<ref>{{cite journal |authors=Freitag CE, Sukov WR, Bryce AH, Berg JV, Vanderbilt CM, Shen W, Smadbeck JB, Greipp PT, Ketterling RP, Jenkins RB, Herrera-Hernandez L, Costello BA, Thompson RH, Boorjian SA, Leibovich BC, Jimenez RE, Murphy SJ, Vasmatzis G, Cheville JC, Gupta S |title=Assessment of isochromosome 12p and 12p abnormalities in germ cell tumors using fluorescence in situ hybridization, single-nucleotide polymorphism arrays, and next-generation sequencing/mate-pair sequencing |journal=Hum Pathol |volume=112 |issue= |pages=20–34 |date=June 2021 |pmid=33798590 |doi=10.1016/j.humpath.2021.03.008 |url=}}</ref> | ||
i(12p) is seen in approximately 80% of male germ cell tumours.<ref>{{cite journal |authors=Bosl GJ, Ilson DH, Rodriguez E, Motzer RJ, Reuter VE, Chaganti RS |title=Clinical relevance of the i(12p) marker chromosome in germ cell tumors |journal=J Natl Cancer Inst |volume=86 |issue=5 |pages=349–55 |date=March 1994 |pmid=8308927 |doi=10.1093/jnci/86.5.349 |url=}}</ref> | i(12p) is seen in approximately 80% of male germ cell tumours.<ref>{{cite journal |authors=Bosl GJ, Ilson DH, Rodriguez E, Motzer RJ, Reuter VE, Chaganti RS |title=Clinical relevance of the i(12p) marker chromosome in germ cell tumors |journal=J Natl Cancer Inst |volume=86 |issue=5 |pages=349–55 |date=March 1994 |pmid=8308927 |doi=10.1093/jnci/86.5.349 |url=}}</ref> | ||
Revision as of 16:34, 13 October 2023
Isochromosome 12p, abbreviated i(12p), a genetic abnormality associated with germ cell tumours.[1]
i(12p) is seen in approximately 80% of male germ cell tumours.[2]
See also
References
- ↑ Freitag CE, Sukov WR, Bryce AH, Berg JV, Vanderbilt CM, Shen W, Smadbeck JB, Greipp PT, Ketterling RP, Jenkins RB, Herrera-Hernandez L, Costello BA, Thompson RH, Boorjian SA, Leibovich BC, Jimenez RE, Murphy SJ, Vasmatzis G, Cheville JC, Gupta S (June 2021). "Assessment of isochromosome 12p and 12p abnormalities in germ cell tumors using fluorescence in situ hybridization, single-nucleotide polymorphism arrays, and next-generation sequencing/mate-pair sequencing". Hum Pathol 112: 20–34. doi:10.1016/j.humpath.2021.03.008. PMID 33798590.
- ↑ Bosl GJ, Ilson DH, Rodriguez E, Motzer RJ, Reuter VE, Chaganti RS (March 1994). "Clinical relevance of the i(12p) marker chromosome in germ cell tumors". J Natl Cancer Inst 86 (5): 349–55. doi:10.1093/jnci/86.5.349. PMID 8308927.