Prenatal diagnosis of an interstitial deletion of 10q (10q11.21 → q21.1): Array comparative genomic hybridization characterization and literature review

被引:2
作者
Chen, Chih-Ping [1 ,2 ,3 ,4 ,5 ,6 ,7 ]
Su, Yi-Ning [8 ]
Chern, Schu-Rern [2 ]
Wu, Peih-Shan [9 ]
Su, Jun-Wei [1 ,10 ]
Town, Dai-Dyi [1 ]
Wang, Wayseen [2 ,11 ]
机构
[1] Mackay Mem Hosp, Dept Obstet & Gynecol, Taipei, Taiwan
[2] Mackay Mem Hosp, Dept Med Res, Taipei, Taiwan
[3] Mackay Med Coll, Dept Med, New Taipei City, Taiwan
[4] Asia Univ, Dept Biotechnol, Taichung, Taiwan
[5] China Med Univ, Sch Chinese Med, Coll Chinese Med, Taichung, Taiwan
[6] Natl Yang Ming Univ, Inst Clin & Community Hlth Nursing, Taipei 112, Taiwan
[7] Natl Yang Ming Univ, Sch Med, Dept Obstet & Gynecol, Taipei 112, Taiwan
[8] Taipei Med Univ, Coll Med, Sch Med, Dept Obstet & Gynecol, Taipei, Taiwan
[9] Gene Biodesign Co Ltd, Taipei, Taiwan
[10] China Med Univ Hosp, Dept Obstet & Gynecol, Taichung, Taiwan
[11] Tatung Univ, Dept Bioengn, Taipei 104, Taiwan
来源
TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY | 2012年 / 51卷 / 04期
关键词
LONG ARM; COCKAYNE-SYNDROME; MYASTHENIC SYNDROME; MENTAL-RETARDATION; GENE POLYMORPHISMS; MUTANT ALLELES; EPISODIC APNEA; MUTATIONS; ASSOCIATION; DISEASE;
D O I
10.1016/j.tjog.2012.09.032
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
[No abstract available]
引用
收藏
页码:672 / 676
页数:5
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