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Difference between revisions of "Isochromosome 12p"
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Can be detect with NGS and or FISH.<ref>{{cite journal |authors=Fichtner A, Richter A, Filmar S, Gaisa NT, Schweyer S, Reis H, Nettersheim D, Oing C, Gayer FA, Leha A, Küffer S, Ströbel P, Kaulfuß S, Bremmer F |title=The detection of isochromosome i(12p) in malignant germ cell tumours and tumours with somatic malignant transformation by the use of quantitative real-time polymerase chain reaction |journal=Histopathology |volume=78 |issue=4 |pages=593–606 |date=March 2021 |pmid=32970854 |doi=10.1111/his.14258 |url=}}</ref><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> | Can be detect with NGS and or FISH.<ref>{{cite journal |authors=Fichtner A, Richter A, Filmar S, Gaisa NT, Schweyer S, Reis H, Nettersheim D, Oing C, Gayer FA, Leha A, Küffer S, Ströbel P, Kaulfuß S, Bremmer F |title=The detection of isochromosome i(12p) in malignant germ cell tumours and tumours with somatic malignant transformation by the use of quantitative real-time polymerase chain reaction |journal=Histopathology |volume=78 |issue=4 |pages=593–606 |date=March 2021 |pmid=32970854 |doi=10.1111/his.14258 |url=}}</ref><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> | ||
==See also== | ==See also== | ||
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==References== | ==References== | ||
{{Reflist| | {{Reflist|2}} | ||
[[Category:Molecular pathology]] | [[Category:Molecular pathology]] | ||
[[Category:Genitourinary pathology]] | [[Category:Genitourinary pathology]] | ||