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Frequent breakpoints of focal deletion and uniparental diso..:
Haruta, Masayuki
;
Arai, Yasuhito
;
Okita, Hajime
...
Genes, Chromosomes and Cancer. 60 (2021) 8 - p. 546-558 , 2021
Link:
https://doi.org/10.1002/gcc.22952
RT Journal T1
Frequent breakpoints of focal deletion and uniparental disomy in 22q11.1 or 11.2 segmental duplication region reveal distinct tumorigenesis in rhabdoid tumor of the kidney
UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_gcc.22952&Exemplar=1&LAN=DE A1 Haruta, Masayuki A1 Arai, Yasuhito A1 Okita, Hajime A1 Tanaka, Yukichi A1 Takimoto, Tetsuya A1 Kamijo, Takehiko A1 Oue, Takaharu A1 Souzaki, Ryota A1 Taguchi, Tomoaki A1 Kuwahara, Yasumichi A1 Chin, Motoaki A1 Nakadate, Hisaya A1 Hiyama, Eiso A1 Ishida, Yasushi A1 Koshinaga, Tsugumichi A1 Kaneko, Yasuhiko PB Wiley YR 2021 SN 1045-2257 SN 1098-2264 JF Genes, Chromosomes and Cancer VO 60 IS 8 SP 546 OP 558 LK http://dx.doi.org/https://doi.org/10.1002/gcc.22952 DO https://doi.org/10.1002/gcc.22952 SF ELIB - SuUB Bremen
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