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A recurrent deletion syndrome at chromosome bands 2p11.2-2p12 flanked by segmental duplications at the breakpoints and including REEP1

机译：2p11.2-2p12染色体带的反复缺失综合症，在断点处侧接节段重复，包括REEP1

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Stevens, Servi J. C.; Blom, Eveline W.; Siegelaer, Ingrid T. J.; Smeets, Eric E. J. G. L.;
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1. A recurrent deletion syndrome at chromosome bands 2p11.2-2p12 flanked by segmental duplications at the breakpoints and including REEP1 [J] . Stevens Servi J. C., Blom Eveline W., Siegelaer Ingrid T. J., European journal of human genetics: EJHG . 2015,第4期

机译：2p11.2-2p12染色体带的反复缺失综合症，在断点处侧接节段重复，包括REEP1
2. Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s). [J] . Valero MC, de-Luis O, Cruces J, Genomics . 2000,第1期

机译：小鼠染色体5G上人7q11.23区和直系同源区的精细比较图谱：在进化反转的断点处出现了Williams-Beuren综合征缺失侧翼的低拷贝重复序列。
3. Duplication or amplification of chromosome band 11q23, including the unrearranged MLL gene, is a recurrent abnormality in therapy-related MDS and AML, and is closely related to mutation of the TP53 gene and to previous therapy with alkylating agents. [J] . Andersen MK, Christiansen DH, Kirchhoff M, Genes, Chromosomes and Cancer . 2001,第1期

机译：包括未重排的MLL基因在内的11q23染色体带的复制或扩增是与治疗相关的MDS和AML的复发异常，并且与TP53基因的突变以及以前使用烷化剂的治疗密切相关。
4. Tandem Duplications, Segmental Duplications and Deletions, and Their Applications [C] . Binhai Zhu International Computer Science Symposium in Russia . 2020

机译：串联重复，分段重复和删除及其应用
5. Genetic Functions of Tbx1 in Mouse Models of 22q11.2 Deletion and Duplication Syndromes [D] . Hasten, Erica 2019

机译：Tbx1在22q11.2删除和复制综合征小鼠模型中的遗传功能。
6. A recurrent deletion syndrome at chromosome bands 2p11.2-2p12 flanked by segmental duplications at the breakpoints and including REEP1 [O] . Servi J C Stevens, Eveline W Blom, Ingrid T J Siegelaer, 2015

机译：2p11.2-2p12染色体带的反复缺失综合症在断点处侧接节段重复包括REEP1
7. Traffic of genetic information between segmental duplications flanking the typical 22q11.2 deletion in velo-cardio-facial syndrome/DiGeorge syndrome [O] . Pavlicek, Adam, House, Reniqua, Gentles, Andrew J., 2005

机译：腔-心-面综合征/ DiGeorge综合征中典型的22q11.2缺失旁的节段重复之间的遗传信息运输

A recurrent deletion syndrome at chromosome bands 2p11.2-2p12 flanked by segmental duplications at the breakpoints and including REEP1

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