RECURRENT DISTAL 16Q DUPLICATION AND TERMINAL 22Q DELETION: PRENATAL DIAGNOSIS AND GENETIC COUNSELING

被引:3
|
作者
Chen, Chih-Ping [1 ,2 ,3 ,4 ,7 ,8 ]
Huang, Ming-Chao [1 ]
Su, Yi-Ning [5 ]
Tsai, Fuu-Jen [8 ,9 ,10 ]
Wu, Pei-Chen [1 ]
Lee, Chen-Chi [1 ]
Town, Dai-Dyi [1 ]
Pan, Chen-Wen [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, Inst Clin & Community Hlth Nursing, Sch Med, 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 Genet, Taichung, Taiwan
[10] China Med Univ Hosp, Dept Med Res, Taichung, Taiwan
来源
关键词
CHROMOSOME ANALYSIS; TRISOMY; 16Q; COUPLES; REARRANGEMENTS; ABNORMALITIES; MISCARRIAGES; SPECTRUM; CARRIERS;
D O I
10.1016/S1028-4559(10)60117-9
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:544 / 547
页数:4
相关论文
共 50 条
  • [1] 22Q DISTAL DUPLICATION SYNDROME
    RIVERA, H
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1989, 34 (04): : 616 - 616
  • [2] Prenatal diagnosis and molecular cytogenetic characterization of de novo distal 5p deletion and distal 22q duplication
    Chen, Chih-Ping
    Huang, Jian-Pei
    Chern, Schu-Rern
    Wu, Peih-Shan
    Chen, Shin-Wen
    Wu, Fang-Tzu
    Chen, Wen-Lin
    Lee, Meng-Shan
    Wang, Wayseen
    TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2020, 59 (01): : 140 - 145
  • [3] DUPLICATION OF 16Q AND DELETION OF 15Q
    NYHAN, WL
    MASCARELLO, J
    BARSHOP, B
    DOROSKI, D
    HIRSCHHORN, K
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1989, 34 (02): : 183 - 186
  • [4] Interstitial deletion involving 22q(13): a phenocopy of the terminal 22q(13) deletion syndrome?
    Vasudevan, PC
    Walker, DA
    Kulak, S
    Yobb, T
    Wilson, HL
    Artifoni, L
    Dallapiccola, B
    Crolla, JA
    Maloney, V
    Quarrell, OWJ
    McDermid, HE
    JOURNAL OF MEDICAL GENETICS, 2004, 41 : S55 - S55
  • [5] 22Q DUPLICATION VS DELETION - A PHENOTYPIC PARADOX
    HIGGINS, JV
    TORIELLO, H
    KOHUT, G
    CYTOGENETICS AND CELL GENETICS, 1995, 71 (04): : 394 - 394
  • [6] 22Q DUPLICATION VERSUS DELETION - A PHENOTYPIC PARADOX
    HIGGINS, JV
    KOHUT, G
    AMERICAN JOURNAL OF HUMAN GENETICS, 1995, 57 (04) : 726 - 726
  • [7] Prenatal diagnosis and molecular cytogenetic characterization of a proximal deletion of 22q (22q11.2→q11.21)
    Chen, Chih-Ping
    Ko, Tsang-Ming
    Su, Yi-Ning
    Su, Jun-Wei
    Chen, Yu-Ting
    Lee, Chen-Chi
    Chen, Li-Feng
    Wang, Wayseen
    TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2013, 52 (01): : 147 - 151
  • [8] Prenatal diagnosis of partial trisomy 16q and distal 22q13 deletion associated with dolichocephaly and frontal bossing on second-trimester ultrasound
    Chen, CP
    Hsu, CY
    Huang, JK
    Lee, CC
    Chen, WL
    Wang, W
    PRENATAL DIAGNOSIS, 2005, 25 (10) : 964 - 966
  • [9] A 22q terminal deletion detectable only by FISH
    Conners, S
    Howell, RT
    Bluett, NH
    McDermott, A
    JOURNAL OF MEDICAL GENETICS, 1999, 36 : S52 - S52
  • [10] ANALYSIS OF A DE-NOVO TANDEM DUPLICATION OF DISTAL 22Q
    HARRIS, DJ
    PASZTOR, LM
    CYTOGENETICS AND CELL GENETICS, 1993, 63 (04): : 252 - 252