Implication of screening for FMR1 and FMR2 gene mutation in individuals with nonspecific mental retardation in Taiwan.

被引:0
|
作者
Tzeng, CC
Tzeng, PY
Sun, HS
Chen, RM
Lin, SJ
机构
[1] Natl Cheng Kung Univ Hosp, Dept Pathol, Tainan, Taiwan
[2] Natl Cheng Kung Univ Hosp, Dept Mol Med, Tainan, Taiwan
[3] Natl Cheng Kung Univ Hosp, Dept Pediat, Tainan, Taiwan
关键词
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
2319
引用
收藏
页码:A410 / A410
页数:1
相关论文
共 50 条
  • [41] 华南地区不明原因智力低下患者 FMR1和 FMR2基因突变分析
    段现来
    刘超
    李啬夫
    石奕武
    易咏红
    廖卫平
    中华神经医学杂志, 2015, 14 (05)
  • [42] Specific effect of the fragile-X mental retardation-1 gene (FMR1) on white matter microstructure
    Green, Tamar
    Barnea-Goraly, Naama
    Raman, Mira
    Hall, Scott S.
    Lightbody, Amy A.
    Bruno, Jennifer L.
    Quintin, Eve-Marie
    Reiss, Allan L.
    BRITISH JOURNAL OF PSYCHIATRY, 2015, 207 (02) : 143 - 148
  • [43] Secondary structure and dynamics of the r(CGG) repeat in the mRNA of the fragile X mental retardation 1 (FMR1) gene
    Zumwalt, Marta
    Ludwig, Anna
    Hagerman, Paul J.
    Dieckmann, Thorsten
    RNA BIOLOGY, 2007, 4 (02) : 93 - 100
  • [44] AGG interspersion analysis of the FMR1 CGG repeats in mental retardation of unspecific cause
    Poon, PMK
    Chen, QL
    Zhong, N
    Lam, STS
    Lai, KYC
    Wong, CK
    Pang, CP
    CLINICAL BIOCHEMISTRY, 2006, 39 (03) : 244 - 248
  • [45] HIGH FREQUENCY OF INTERMEDIATE ALLELES OF FRAGILE X MENTAL RETARDATION 1 GENE (FMR1) IN CANDIDATES FOR OOCYTE DONATION
    Guillen, J.
    Vassena, R.
    Vernaeve, V.
    Rodriguez, A.
    FERTILITY AND STERILITY, 2015, 104 (03) : E76 - E76
  • [46] A POINT MUTATION IN THE FMR-1 GENE ASSOCIATED WITH FRAGILE-X MENTAL-RETARDATION
    DEBOULLE, K
    VERKERK, AJMH
    REYNIERS, E
    VITS, L
    HENDRICKX, J
    VANROY, B
    VANDENBOS, F
    DEGRAAFF, E
    OOSTRA, BA
    WILLEMS, PJ
    NATURE GENETICS, 1993, 3 (01) : 31 - 35
  • [47] A new PCR assay useful for screening of FRAXE/FMR2 mental impairment among males
    Santos, CB
    Lima, MAC
    Pimentel, MMG
    HUMAN MUTATION, 2001, 18 (02) : 157 - 162
  • [48] FIRING PROPERTY OF INFERIOR COLLICULUS NEURONS AFFECTED BY FMR1 GENE MUTATION
    Brittany Mott
    SUN Wei
    JournalofOtology, 2014, 9 (02) : 86 - 90
  • [49] Severe Hunter Syndrome (Mucopolysaccharidosis II) Phenotype Secondary to Large Deletion in the X Chromosome Encompassing IDS, FMR1, and AFF2 (FMR2)
    Burruss, Day M.
    Wood, Tim C.
    Espinoza, Lesby
    Dwivedi, Alka
    Holden, Kenton R.
    JOURNAL OF CHILD NEUROLOGY, 2012, 27 (06) : 786 - 790
  • [50] Establishment of Reporter Lines for Detecting Fragile X Mental Retardation (FMR1) Gene Reactivation in Human Neural Cells
    Li, Meng
    Zhao, Huashan
    Ananiev, Gene E.
    Musser, Michael T.
    Ness, Kathryn H.
    Maglaque, Dianne L.
    Saha, Krishanu
    Bhattacharyya, Anita
    Zhao, Xinyu
    STEM CELLS, 2017, 35 (01) : 158 - 169