18Q-SYNDROME RESULTING FROM A TDIC(14P - 18Q)

被引：7
|
作者：
LAMBERT, JC [1 ]
FERRARI, M [1 ]
BERGONDI, C [1 ]
GALLIANA, A [1 ]
AYRAUD, N [1 ]
机构：
[1] HOP INTERCOMMUNAL FREJUS ST RAPHAEL,SERV PEDIAT,F-83608 FREJUS,FRANCE
来源：
HUMAN GENETICS | 1979年 / 48卷 / 01期
关键词：
D O I：
10.1007/BF00273275
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：61 / 66
页数：6
相关论文
共 50 条
  • [31] Hearing impairment in 18q deletion syndrome
    Jayarajan, V
    Swan, IRC
    Patton, MA
    JOURNAL OF LARYNGOLOGY AND OTOLOGY, 2000, 114 (12): : 963 - 966
  • [32] Identification of an 18q-syndrome paitent who is mosaic for two differention deletions of 18q.
    Reveles, XT
    Cody, JD
    Thompson, NM
    Leach, RJ
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 142 - 142
  • [33] Monosomy 18q syndrome and atypical Rett syndrome in a girl with an interstitial deletion (18)(q21.1q22.3)
    Gustavsson, P
    Kimber, E
    Wahlström, J
    Annerén, G
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1999, 82 (04): : 348 - 351
  • [34] DELETION 9P, DUPLICATION 18Q IN 2 SISTERS RESULTING FROM A MATERNAL (9-18) (P22-Q21.3) TRANSLOCATION
    TAYEL, SM
    KURCZYNSKI, TW
    CASPERSON, S
    MCCORQUODALE, MM
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1988, 31 (04): : 853 - 861
  • [35] 18P - SYNDROME RESULTING FROM TRANSLOCATION (13Q-18Q) IN A MILDLY AFFECTED ADULT MALE
    MOEDJONO, SJ
    FUNDERBURK, SJ
    SPARKES, RS
    JOURNAL OF MEDICAL GENETICS, 1979, 16 (05) : 399 - 402
  • [36] FAMILIAL PARTIAL DISTAL 18Q (18Q22-18Q23) TRISOMY
    DEMUELENAERE, A
    FRYNS, JP
    VANDENBERGHE, H
    ANNALES DE GENETIQUE, 1981, 24 (03): : 184 - 186
  • [37] Intelligence Associated with Deletion Size in Children with 18q-Syndrome
    Nora M Thompson
    Jannine D Cody
    Erin McClure
    Celia I Kaye
    Robin J Leach
    Pediatric Research, 1999, 45 : 142 - 142
  • [38] 18Q-SYNDROME - NEUROFIBRILLARY TANGLES WITHOUT NEURITIC PLAQUES
    HALLIDAY, WC
    CHUDLEY, AE
    JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1989, 48 (03): : 308 - 308
  • [39] ISOCHROMOSOME (18Q) IN SIBLINGS
    KRUGER, G
    GOTZ, J
    DUNKER, H
    PELZ, L
    CLINICAL GENETICS, 1987, 32 (04) : 249 - 253
  • [40] Gene expression patterns in cell lines from patients with 18q-syndrome
    Wang, ZQ
    Cody, JD
    Leach, RJ
    O'Connell, P
    HUMAN GENETICS, 1999, 104 (06) : 467 - 475
12345