IDENTIFICATION IMPRINTING GENE EXPRESSION AT 15Q11-Q13 REGION IN ANGELMAN SYNDROME

被引：0
|
作者：
Vijayakumar, P. [1 ]
机构：
[1] Bharathiar Univ, Dept Human Genet & Mol Biol, Coimbatore, Tamil Nadu, India
来源：
PARKINSONISM & RELATED DISORDERS | 2018年 / 46卷
关键词：
Angelman Syndrome (AS); Chromosomal Alteration; UBE3A gene and DNA Methylation;
D O I：
暂无
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
P-058
引用
收藏
页码：E53 / E54
页数：2
相关论文
共 50 条
  • [1] Mosaic paternal uniparental isodisomy of 15q11-q13 region causing Angelman phenotype
    Narayanan, Dhanya Lakshmi
    Ranganath, Prajnya
    Balakrishnan, Surya
    Dalal, Ashwin
    [J]. CLINICAL DYSMORPHOLOGY, 2019, 28 (04) : 202 - 204
  • [2] ANGELMANS SYNDROME MAPS TO 15Q11-Q13
    MALCOLM, S
    LEDBETTER, DH
    WEBB, T
    RUTLAND, P
    MIDDLETONPRICE, HR
    PEMBREY, ME
    [J]. CYTOGENETICS AND CELL GENETICS, 1989, 51 (1-4): : 1038 - 1039
  • [3] Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes
    Kalsner, Louisa
    Chamberlain, Stormy J.
    [J]. PEDIATRIC CLINICS OF NORTH AMERICA, 2015, 62 (03) : 587 - +
  • [4] Prenatal diagnosis of Prader-Willi syndrome and Angelman syndrome for fetuses with suspicious deletion of chromosomal region 15q11-q13
    Chang, Chia-Wei
    Hsu, Hui-Kuo
    Kao, Chiu-Ching
    Huang, Jyun-Yuan
    Kuo, Pao-Lin
    [J]. INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS, 2014, 125 (01) : 18 - 21
  • [5] PHYSICAL MAPPING STUDIES AT D15S10 - IMPLICATIONS FOR CANDIDATE GENE IDENTIFICATION IN THE ANGELMAN SYNDROME/PRADER-WILLI SYNDROME CHROMOSOME REGION OF 15Q11-Q13
    WOODAGE, T
    LINDEMAN, R
    DENG, ZM
    FIMMEL, A
    SMITH, A
    TRENT, RJ
    [J]. GENOMICS, 1994, 19 (01) : 170 - 172
  • [6] Angelman syndrome methylation screening of 15q11-q13 in institutionalized individuals with severe mental retardation
    Aquino, NHC
    Bastos, E
    Fonseca, LCG
    Llerena, JC
    [J]. GENETIC TESTING, 2002, 6 (02): : 129 - 131
  • [7] ANGELMAN SYNDROME - VALIDATION OF MOLECULAR CYTOGENETIC ANALYSIS OF CHROMOSOME 15Q11-Q13 FOR DELETION DETECTION
    WHITE, L
    KNOLL, JHM
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 56 (01): : 101 - 105
  • [8] CHARACTERIZATION OF A DNA-SEQUENCE FAMILY IN THE PRADER-WILLI ANGELMAN SYNDROME CHROMOSOME REGION IN 15Q11-Q13
    DITTRICH, B
    KNOBLAUCH, H
    BUITING, K
    HORSTHEMKE, B
    [J]. GENOMICS, 1993, 16 (01) : 269 - 271
  • [9] Identification of a silencing element in the human 15q11-q13 imprinting center by using transgenic Drosophila
    Lyko, F
    Buiting, K
    Horsthemke, B
    Paro, R
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (04) : 1698 - 1702
  • [10] A COMPLETE YAC CONTIG OF THE PRADER-WILLI/ANGELMAN CHROMOSOME REGION (15Q11-Q13) AND REFINED LOCALIZATION OF THE SNRPN GENE
    MUTIRANGURA, A
    JAYAKUMAR, A
    SUTCLIFFE, JS
    NAKAO, M
    MCKINNEY, MJ
    BUITING, K
    HORSTHEMKE, B
    BEAUDET, AL
    CHINAULT, AC
    LEDBETTER, DH
    [J]. GENOMICS, 1993, 18 (03) : 546 - 552
12345