Further case report of a child with a 9q34 deletion and a review of the reported cases

被引：3
作者：
Kannu, P [1 ]
Winship, I [1 ]
Aftimos, S [1 ]
机构：
[1] Auckland Hosp, No Reg Genet Serv, Auckland, New Zealand
来源：
AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 2005年 / 133A卷 / 02期
关键词：
D O I：
10.1002/ajmg.a.30507
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：219 / 221
页数：3
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共 9 条
  • [1] Subtelomeric rearrangements detected in patients with idiopathic mental retardation
    Anderlid, BM
    Schoumans, J
    Annerén, G
    Sahlén, S
    Kyllerman, M
    Vujic, M
    Hagberg, B
    Blennow, E
    Nordenskjöld, M
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 107 (04): : 275 - 284
  • [2] A report of a child with a deletion (9)(q34.3): A recognisable phenotype?
    Ayyash, H
    Mueller, R
    Maltby, E
    Horsfield, P
    Telford, N
    Tyler, R
    [J]. JOURNAL OF MEDICAL GENETICS, 1997, 34 (07) : 610 - 612
  • [3] Cryptic terminal deletion of chromosome 9q34: a novel cause of syndromic obesity in childhood?
    Cormier-Daire, V
    Molinari, F
    Rio, M
    Raoul, O
    de Blois, MC
    Romana, S
    Vekemans, M
    Munnich, A
    Colleaux, L
    [J]. JOURNAL OF MEDICAL GENETICS, 2003, 40 (04) : 300 - 303
  • [4] Clinical studies on submicroscopic subtelomeric rearrangements: a checklist
    de Vries, BBA
    White, SM
    Knight, SJL
    Regan, R
    Homfray, T
    Young, ID
    Super, M
    McKeown, C
    Splitt, M
    Quarrell, OWJ
    Trainer, AH
    Niermeijer, MF
    Malcolm, S
    Flint, J
    Hurst, JA
    Winter, RM
    [J]. JOURNAL OF MEDICAL GENETICS, 2001, 38 (03) : 145 - 150
  • [5] 9q34.3 deletion syndrome in three unrelated children
    Iwakoshi, M
    Okamoto, N
    Harada, N
    Nakamura, T
    Yamamori, S
    Fujita, H
    Niikawa, N
    Matsumoto, N
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2004, 126A (03) : 278 - 283
  • [6] Subtle chromosomal rearrangements in children with unexplained mental retardation
    Knight, SJL
    Regan, R
    Nicod, A
    Horsley, SW
    Kearney, L
    Homfray, T
    Winter, RM
    Bolton, P
    Flint, J
    [J]. LANCET, 1999, 354 (9191) : 1676 - 1681
  • [7] Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformations
    Rossi, E
    Piccini, F
    Zollino, M
    Neri, G
    Caselli, D
    Tenconi, R
    Castellan, C
    Carrozzo, R
    Danesino, C
    Zuffardi, O
    Ragusa, A
    Castiglia, L
    Galesi, O
    Greco, D
    Romano, C
    Pierluigi, M
    Perfumo, C
    Di Rocco, M
    Faravelli, F
    Bricarelli, FD
    Bonaglia, M
    Bedeschi, M
    Borgatti, R
    [J]. JOURNAL OF MEDICAL GENETICS, 2001, 38 (06) : 417 - 420
  • [8] INFANT WITH MULTIPLE CONGENITAL-ANOMALIES AND DELETION (9)(Q34.3)
    SCHIMMENTI, LA
    BERRY, SA
    TUCHMAN, M
    HIRSCH, B
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1994, 51 (02): : 140 - 142
  • [9] Subtelomeric deletions of chromosome 9q:: A novel microdeletion syndrome
    Stewart, DR
    Huang, A
    Faravelli, F
    Anderlid, BM
    Medne, L
    Ciprero, K
    Kaur, M
    Rossi, E
    Tenconi, R
    Nordenskjöld, M
    Gripp, KW
    Nicholson, L
    Meschino, WS
    Capua, E
    Quarrell, OWJ
    Flint, J
    Irons, M
    Giampietro, PF
    Schowalter, DB
    Zaleski, CA
    Malacarne, M
    Zackai, EH
    Spinner, NB
    Krantz, ID
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2004, 128A (04) : 340 - 351
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