Assessment of subtelomeric regions of children with autism: Detection of a 2q deletion.

被引:0
|
作者
Wolff, DJ
Clifton, K
Charles, J
机构
[1] Med Univ S Carolina, Dept Pathol & Lab Med, Charleston, SC 29425 USA
[2] Med Univ S Carolina, Dept Med Lab Sci, Charleston, SC 29425 USA
[3] Med Univ S Carolina, Dept Pediat, Charleston, SC 29425 USA
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
857
引用
收藏
页码:162 / 162
页数:1
相关论文
共 50 条
  • [21] TERMINAL 2q DELETION AND PARTIAL TRISOMY CHROMOSOME 15q: A CLINICAL AND CYTOGENETIC STUDY
    El-Bassyouni, H. T.
    El-Gerzawy, A. M. S.
    Mohamed, A. M.
    Kamel, A. K.
    Hussein, H. A.
    Thomas, M. M.
    El-Ruby, M.
    GENETIC COUNSELING, 2014, 25 (02): : 151 - 158
  • [22] Autism in children with 22Q11.2 deletion syndrome - Reply
    Vorstman, Jacob A. S.
    Morcus, Monique E. J.
    van Engeland, Herman
    JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY, 2007, 46 (04): : 434 - 435
  • [23] Autism phenotype in children with 22Q11 deletion syndrome
    Vorstman, JAS
    Morcus, MEJ
    Swaab-Barneveld, H
    Heineman-de Boer, JA
    Duijff, SN
    Jansen, P
    Beemer, FA
    van Engeland, H
    AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2004, 130B (01): : 73 - 73
  • [25] Fine mapping of a susceptibility region and candidate gene studies on chromosome 2q in autism
    Gallagher, L
    Ennis, S
    Kearney, G
    Fitzgerald, M
    Stallings, R
    Barton, D
    Green, AJ
    Gill, M
    AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 114 (07): : 729 - 729
  • [26] A PRESUMPTIVE TRANSLOCATION 1P,2Q RESULTING IN DUPLICATION-1P AND DELETION-2Q
    HALAL, F
    VEKEMANS, M
    DERKALOUSTIAN, VM
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1989, 32 (03): : 376 - 379
  • [27] Psychiatric disorders and autism in young children with 22q11.2 deletion syndrome compared to children with idiopathic autism
    Serur, Yaffa
    Frumer, Dafna Sofrin
    Daon, Keren
    Sobol-Havia, Dolly
    Weinberger, Ronnie
    Shulman, Cory
    Gothelf, Doron
    EUROPEAN PSYCHIATRY, 2019, 55 : 116 - 121
  • [28] PARTIAL DUPLICATION 14Q DELETION 2Q IN 2 SIBS DUE TO T(2-14) (Q37.1-Q31.2) PAT
    DELAFUENTE, AA
    GERSSENSCHOORL, KBJ
    BREED, ASPM
    ANNALES DE GENETIQUE, 1988, 31 (04): : 254 - 257
  • [29] Detection of an unexpected subtelomeric 15q26.2→qter deletion in a little girl:: Clinical and cytogenetic studies
    Pinson, L
    Perrin, A
    Plouzennec, C
    Parent, P
    Metz, C
    Collet, M
    Le Bris, MJ
    Douet-Guilbert, N
    Morel, F
    De Braekeleer, M
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2005, 138A (02) : 160 - 165
  • [30] A genomewide screen for autism:: Strong evidence for linkage to chromosomes 2q, 7q, and 16p
    Palferman, S
    Matthews, N
    Turner, M
    Moore, J
    Hervas, A
    Aubin, A
    Wallace, S
    Michelotti, J
    Wainhouse, C
    Paul, A
    Thompson, E
    Gupta, R
    Garner, C
    Murin, M
    Freitag, C
    Ryder, N
    Cottington, E
    Parr, J
    Pickles, A
    Rutter, M
    Bailey, A
    Barnby, G
    Lamb, JA
    Marlow, A
    Scudder, P
    Monaco, AP
    Baird, G
    Cox, A
    Docherty, Z
    Warburton, P
    Green, EP
    Abbs, SJ
    Le Couteur, A
    McConachie, HR
    Berney, T
    Kelly, TP
    De Vries, PJ
    Bolton, PF
    Green, J
    Gilchrist, A
    Whittacker, J
    Bolton, B
    Packer, R
    Maestrini, E
    Blasi, F
    Van Engeland, H
    De Jonge, MV
    Kemner, C
    Klauck, SM
    Beyer, KS
    AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (03) : 570 - 581