MECP2 gene rearrangements in three males with mental retardation and Rett-like features

被引：0
|
作者：
Gali, P.
Gak, E.
Lerman, S.
Reznik, H.
Michelson-Kerman, M.
Pras, E.
Ben Zeev, B.
机构：
来源：
ANNALS OF NEUROLOGY | 2007年 / 62卷
关键词：
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：
引用
收藏
页码：S123 / S123
页数：1
相关论文
共 50 条
  • [1] MECP2 gene analysis in classical Rett syndrome and in patients with Rett-like features
    Auranen, M
    Vanhala, R
    Vosman, M
    Levander, M
    Varilo, T
    Hietala, M
    Riikonen, R
    Peltonen, L
    Järvelä, I
    [J]. NEUROLOGY, 2001, 56 (05) : 611 - 617
  • [2] MECP2 gene analysis in Japanese patients with classical and variant Rett syndromes and with Rett-like features.
    Yamada, Y
    Miura, K
    Kumagai, T
    Ohki, T
    Hayakawa, C
    Miyazaki, S
    Matsumoto, A
    Nomura, N
    Sonta, S
    Yamanaka, T
    Wakamatsu, N
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 646 - 646
  • [3] Whole Exome Sequencing of Patients with Rett-like Features Negative for MECP2 Mutations
    Olson, H. E.
    Khwaja, O.
    Poduri, A.
    Kaufmann, W.
    [J]. ANNALS OF NEUROLOGY, 2013, 74 : S160 - S161
  • [4] A mutation in the Rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males
    Meloni, I
    Bruttini, M
    Longo, I
    Mari, F
    Rizzolio, F
    D'Adamo, P
    Denvriendt, K
    Fryns, JP
    Toniolo, D
    Renieri, A
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 982 - 985
  • [5] A Rett syndrome MECP2 mutation that causes mental retardation in men
    Dotti, MT
    Orrico, A
    De Stefano, N
    Battisti, C
    Sicurelli, F
    Severi, S
    Lam, CW
    Galli, L
    Sorrentino, V
    Federico, A
    [J]. NEUROLOGY, 2002, 58 (02) : 226 - 230
  • [6] MECP2 and mental retardation
    Gilgenkrantz, S
    Bourdon, V
    [J]. M S-MEDECINE SCIENCES, 2001, 17 (6-7): : 810 - 812
  • [7] Gross rearrangements in the MECP2 gene in three patients with Rett syndrome:: Implications for routine diagnosis of Rett syndrome
    Schollen, E
    Smeets, E
    Deflem, E
    Fryns, JP
    Matthijs, G
    [J]. HUMAN MUTATION, 2003, 22 (02) : 116 - 120
  • [8] Clinical studies and analysis of the Rett syndrome gene (MECP2) in children with mental retardation in the Greek population
    Psoni, Stavroula
    Traeger-Synodinos, Joanne
    Sofocleous, Christalena
    Kitsiou-Tzeli, Sophia
    Mavrou, Ariadni
    Kanavakis, Emmanuel
    Fryssira, Helen
    [J]. PEDIATRICS, 2008, 121 : S117 - S118
  • [9] Rett syndrome and the MECP2 gene
    Webb, T
    Latif, F
    [J]. JOURNAL OF MEDICAL GENETICS, 2001, 38 (04) : 217 - 223
  • [10] Gross rearrangements in the MECP2 gene in two patients with Rett syndrome.
    Schollen, E
    Deflem, E
    Smeets, E
    Fryns, JP
    Matthijs, G
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 550 - 550
12345