PRENATAL DIAGNOSIS AND MOLECULAR CYTOGENETIC CHARACTERIZATION OF A SMALL SUPERNUMERARY MARKER CHROMOSOME DERIVED FROM CHROMOSOME 22

被引：7
作者：
Chen, Chih-Ping [1 ,2 ,3 ,4 ,7 ,8 ]
Lin, Chyi Chyang [9 ]
Su, Yi Ning [5 ]
Tsai, Fuu Jen [8 ,9 ,10 ]
Chern, Schu Rern [2 ]
Lee, Chen Chi [1 ]
Chen, Wen Ling [1 ]
Chen, Li Feng [1 ]
Wu, Pei-Chen [1 ]
Wang, Wayseen [2 ,6 ]
机构：
[1] Mackay Mem Hosp, Dept Obstet & Gynecol, Taipei, Taiwan
[2] Mackay Mem Hosp, Dept Med Res, Taipei, Taiwan
[3] Natl Yang Ming Univ, Sch Med, Inst Clin & Community Hlth Nursing, Taipei 112, Taiwan
[4] Natl Yang Ming Univ, Sch Med, Dept Obstet & Gynecol, Taipei 112, Taiwan
[5] Natl Taiwan Univ Hosp, Dept Med Genet, Taipei, Taiwan
[6] Tatung Univ, Dept Bioengn, Taipei 104, Taiwan
[7] Asia Univ, Dept Biotechnol, Taichung, Taiwan
[8] China Med Univ, Coll Chinese Med, Sch Chinese Med, Taichung, Taiwan
[9] China Med Univ Hosp, Dept Med Res, Taichung, Taiwan
[10] China Med Univ Hosp, Dept Med Genet, Taichung, Taiwan
来源：
TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY | 2010年 / 49卷 / 03期
关键词：
CAT-EYE SYNDROME; CRITICAL REGION; PHENOTYPE; DNA; TRANSLOCATION; DELINEATION; DISORDERS; MEDIATE; HUMANS; 22Q11;
D O I：
10.1016/S1028-4559(10)60081-2
中图分类号：
R71 [妇产科学];
学科分类号：
100211 ;
摘要：
引用
收藏
页码：381 / 384
页数：4
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