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Confirmation of 6q21–6q22.1 Deletion in Acro-Cardio-Facial Syndrome and Further Delineation of This Contiguous Gene Deletion Syndrome

机译：心脏-面部综合征中6q21-6q22.1缺失的确认以及这种连续基因缺失综合征的进一步描述

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期刊名称 other
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Cindy Hudson; Corbin Schwanke; John P. Johnson; Abdallah F. Elias; Sandy Phillips; Tammy Schwalbe; Mary Tunby; Dongbin Xu;
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年(卷),期 -1(164A),8
年度 -1
页码 2109–2113
总页数 11
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1. Confirmation of 6q21-6q22.1 deletion in Acro-cardio-facial syndrome and further delineation of this contiguous gene deletion syndrome [J] . HudsonC., SchwankeC., JohnsonJ.P., American journal of medical genetics, Part A . 2014,第8期

机译：确认Acro-心血管面部综合征中6q21-6q22.1缺失并进一步描述该连续基因缺失综合征
2. Ectodermal dysplasia-like syndrome with mental retardation due to contiguous gene deletion: further clinical and molecular delineation of del(2q32) syndrome. [J] . Rifai L, Port Lis M, Tabet AC, American journal of medical genetics, Part A . 2010,第1期

机译：由于连续基因缺失而导致智力低下的表皮异型增生样综合征：del（2q32）综合征的进一步临床和分子描述。
3. 5q14.3 Deletion Neurocutaneous Syndrome: Contiguous Gene Syndrome Caused by Simultaneous Deletion of RASA1 and MEF2C: A Progressive Disease [J] . Ilari Rita, Agosta Guillermo, Bacino Carlos American journal of medical genetics, Part A . 2016,第3期

机译：5q14.3删除神经皮肤综合症：RASA1和MEF2C同时删除引起的连续基因综合症：一种进行性疾病
4. On ordered syndromes for multi insertion/deletion error-correcting codes [C] . Manabu Hagiwara IEEE International Symposium on Information Theory . 2016

机译：关于多重插入/删除纠错码的有序校正子
5. Chromosomal mapping of genes encoding human Pur-alpha and Pur-beta: Independent and simultaneous deletions in myelodysplastic syndromes and acute myelogenous leukemia. [D] . Lezon-Geyda, Kimberly Ann. 2001

机译：编码人Pur-alpha和Pur-beta的基因的染色体作图：骨髓增生异常综合症和急性骨髓性白血病的独立和同时缺失。
6. Delineation of a contiguous gene syndrome with multiple exostoses enlarged parietal foramina craniofacial dysostosis and mental retardation caused by deletions in the short arm of chromosome 11. [O] . O. Bartsch, W. Wuyts, W. Van Hul, 1996

机译：由11号染色体短臂缺失引起的具有多个外生糖顶壁孔眼扩大颅面肌发育不良和智力低下的连续基因综合征的描述。
7. Tiling path resolution mapping of constitutional 1p36 deletions by array-CGH: contiguous gene deletion or "deletion with positional effect" syndrome? [O] . Redon, R, Rio, M, Gregory, S, 2005

机译：阵列CGH构成1p36缺失的平铺路径分辨率定位：连续基因缺失还是“具有位置效应的缺失”综合征？

Confirmation of 6q21–6q22.1 Deletion in Acro-Cardio-Facial Syndrome and Further Delineation of This Contiguous Gene Deletion Syndrome

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