Mosaicism for FMR1 and FMR2 deletion:: a new case

被引：12
|
作者：
Fengler, S [1 ]
Fuchs, S [1 ]
König, R [1 ]
Arnemann, J [1 ]
机构：
[1] Johann Wolfgang Goethe Univ Hosp, Inst Human Genet, D-60590 Frankfurt, Germany
来源：
JOURNAL OF MEDICAL GENETICS | 2002年 / 39卷 / 03期
关键词：
D O I：
10.1136/jmg.39.3.200
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：200 / 201
页数：2
相关论文
共 50 条
  • [1] Fragile X syndrome with FMR1 and FMR2 deletion
    Moore, SJ
    Strain, L
    Cole, GF
    Miedzybrodzka, Z
    Kelly, KF
    Dean, JCS
    JOURNAL OF MEDICAL GENETICS, 1999, 36 (07) : 565 - 566
  • [2] FMR1 and FMR2 analysis in autistic population.
    Yamagata, T
    Suwa, K
    Mori, M
    Nakamura, M
    Momoi, MY
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 404 - 404
  • [3] Distribution of FMR1 and FMR2 Repeats in Argentinean Patients with Primary Ovarian Insufficiency
    Daniela Espeche, Lucia
    Chiauzzi, Violeta
    Ferder, Ianina
    Arrar, Mehrnoosh
    Paula Solari, Andrea
    David Bruque, Carlos
    Delea, Marisol
    Belli, Susana
    Soledad Fernandez, Cecilia
    Delia Buzzalino, Noemi
    Hernan Charreau, Eduardo
    Beatriz Dain, Liliana
    GENES, 2017, 8 (08):
  • [4] Instability of the FMR2 trinucleotide repeat region associated with expanded FMR1 alleles
    Brown, TC
    Tarleton, JC
    Go, RCP
    Longshore, JW
    Descartes, M
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1997, 73 (04): : 447 - 455
  • [5] The prevalence of the FMR1 and FMR2 mutations among preschool children with language delay
    Mazzocco, MMM
    Myers, GF
    Hamner, JL
    Panoscha, R
    Shapiro, BK
    Reiss, AL
    JOURNAL OF PEDIATRICS, 1998, 132 (05): : 795 - 801
  • [6] Distribution of FMR1 and FMR2 repeats in Argentinean patients with primary ovarian insufficiency
    Espeche, L. D.
    Chiauzzi, V.
    Ferder, I.
    Arrar, M.
    Solari, A. P.
    Bruque, C. D.
    Delea, M.
    Belli, S.
    Fernandez, C. S.
    Buzzalino, N. D.
    Charreau, E. H.
    Dain, L. B.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 885 - 885
  • [7] Mosaicism for an FMR1 gene deletion in a fragile X female
    Fan, HX
    Booker, JK
    McCandless, SE
    Shashi, V
    Fleming, A
    Farber, RA
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2005, 136A (02) : 214 - 217
  • [8] Implication of screening for FMR1 and FMR2 gene mutation in individuals with nonspecific mental retardation in Taiwan
    Tzeng, CC
    Tzeng, PY
    Sun, HS
    Chen, RM
    Lin, SJ
    DIAGNOSTIC MOLECULAR PATHOLOGY, 2000, 9 (02) : 75 - 80
  • [9] Think About It: FMR1 Gene Mosaicism
    Bonarrigo, Francesca Andrea
    Russo, Silvia
    Vizziello, Paola
    Menni, Francesca
    Cogliati, Francesca
    Giorgini, Valentina
    Monti, Federico
    Milani, Donatella
    JOURNAL OF CHILD NEUROLOGY, 2014, 29 (09) : NP74 - NP77
  • [10] Germinal mosaicism for a deletion of the FMR1 gene leading to fragile X syndrome
    Jiraanont, P.
    Hagerman, R. J.
    Neri, G.
    Zollino, M.
    Murdolo, M.
    Tassone, F.
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2016, 59 (09) : 459 - 462
12345