Chromosome 22q11 deletion and pachygyria characterized by array-based comparative genomic hybridization

被引:12
|
作者
Koolen, DA
Veltman, JA
Renier, WO
Droog, RP
van Kessel, AG
de Vries, BBA
机构
[1] Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
[2] Univ Nijmegen, Med Ctr, Dept Neurol, Nijmegen, Netherlands
[3] Elkerliek Hosp, Dept Pediat, Helmond, Netherlands
关键词
D O I
10.1002/ajmg.a.30377
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:322 / 324
页数:3
相关论文
共 50 条
  • [1] Pachygyria and polymicrogyria in 22q11 deletion syndrome
    Ehara, H
    Maegaki, Y
    Takeshita, K
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2003, 117A (01): : 80 - 82
  • [2] Craniosynostosis and chromosome 22q11 deletion
    Dean, JCS
    de Silva, DC
    Reardon, W
    JOURNAL OF MEDICAL GENETICS, 1998, 35 (04) : 346 - 346
  • [3] Deletion of chromosome 22q11 and pseudohypoparathyroidism
    Craigen, WJ
    Lindsay, EA
    Bricker, JT
    Hawkins, EP
    Baldini, A
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1997, 72 (01): : 63 - 65
  • [4] Chromosome 22q11 deletion and brain structure
    Eliez, S
    Blasey, CM
    BRITISH JOURNAL OF PSYCHIATRY, 2001, 179 : 270 - 270
  • [5] Myopathy in a patient with chromosome 22q11 deletion
    Mongini, T
    Doriguzzi, C
    Arduino, C
    Brusco, A
    Bortolotto, S
    Mutani, R
    Palmucci, L
    NEUROPEDIATRICS, 2001, 32 (02) : 107 - 109
  • [6] Radial aplasia and chromosome 22q11 deletion
    Digilio, MC
    Giannotti, A
    Marino, B
    Guadagni, AM
    Orzalesi, M
    Dallapiccola, B
    JOURNAL OF MEDICAL GENETICS, 1997, 34 (11) : 942 - 944
  • [7] Clinical features of chromosome 22q11 deletion
    Hunter, A
    JOURNAL OF MEDICAL GENETICS, 1998, 35 (04) : 346 - 346
  • [8] Velopharyngeal incompetence and chromosome 22q11 deletion
    Boorman, JG
    Varma, S
    Ogilvie, CM
    LANCET, 2001, 357 (9258): : 774 - 774
  • [9] Array-based comparative genomic hybridization analysis of recurrent chromosome 15q rearrangements
    Sahoo, T
    Shaw, CA
    Young, AS
    Whitehouse, NL
    Schroer, RJ
    Stevenson, RE
    Beaudet, AL
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2005, 139A (02) : 106 - 113
  • [10] Submicroscopic deletion in chromosome 22q11 in trizygous triplet siblings and their father - Clinical variability of 22q11 deletion
    Devriendt, K
    VanHoestenberghe, R
    VanHole, C
    Devlieger, H
    Gewillig, M
    Moerman, P
    VandenBerghe, H
    Fryns, JP
    CLINICAL GENETICS, 1997, 51 (04) : 246 - 249