DOUBLE I(18Q) IN LYMPHOMA

被引：3
|
作者：
MANDAL, AK [1 ]
ROBERTS, SH [1 ]
LAURENCE, KM [1 ]
机构：
[1] UNIV HOSP WALES,INST MED GENET,CARDIFF CF4 4XN,S GLAM,WALES
来源：
CANCER GENETICS AND CYTOGENETICS | 1990年 / 44卷 / 02期
关键词：
D O I：
10.1016/0165-4608(90)90059-J
中图分类号：
R73 [肿瘤学];
学科分类号：
100214 ;
摘要：
引用
收藏
页码：279 / 281
页数：3
相关论文
共 50 条
  • [41] Myelination in children with partial deletions of chromosome 18q
    Lancaster, JL
    Cody, JD
    Andrews, T
    Hardies, LJ
    Hale, DE
    Fox, PT
    AMERICAN JOURNAL OF NEURORADIOLOGY, 2005, 26 (03) : 447 - 454
  • [42] Otologic Characteristics of Individuals With Deletions of Distal 18q
    Perry, Brian P.
    Cody, Jannine D.
    LARYNGOSCOPE, 2014, 124 (11): : 2606 - 2609
  • [43] 一例,46XY,i(18q)综合征
    梁品容
    刘珍
    中华医学遗传学杂志, 1992, (01) : 35 - 35
  • [44] PARTIAL TRISOMY 18Q IN A NEWBORN WITH TYPICAL 18 TRISOMY PHENOTYPE
    FRYNS, JP
    DETAVERNIER, F
    VANFLETEREN, A
    VANDENBERGHE, H
    HUMAN GENETICS, 1978, 44 (02) : 201 - 205
  • [45] The spectrum of growth abnormalities in children with 18q deletions
    Hale, DE
    Cody, JD
    Baillargeon, J
    Schaub, R
    Danney, MM
    Leach, RJ
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (12): : 4450 - 4454
  • [46] Genetic determinants of autism in individuals with deletions of 18q
    Louise O’Donnell
    Bridgette Soileau
    Patricia Heard
    Erika Carter
    Courtney Sebold
    Jon Gelfond
    Daniel E. Hale
    Jannine D. Cody
    Human Genetics, 2010, 128 : 155 - 164
  • [47] DEFINING THE PROXIMAL INTERSTITIAL 18Q DELETION SYNDROME
    CHUDLEY, AE
    KRASIKOV, N
    AMERICAN JOURNAL OF HUMAN GENETICS, 1991, 49 (04) : 259 - 259
  • [48] Prenatal diagnosis of pure distal 18q deletion
    Chen, CP
    Chern, SR
    Hung, FY
    Hsu, CY
    Chang, TY
    Lee, CC
    Town, DD
    Chen, WL
    Chen, LF
    Tzen, CY
    Wang, W
    Ma, R
    PRENATAL DIAGNOSIS, 2006, 26 (02) : 184 - 185
  • [49] Skin manifestations of chromosome 18q deletion syndrome
    Torchia, Daniele
    Schachner, Lawrence A.
    INTERNATIONAL JOURNAL OF DERMATOLOGY, 2015, 54 (08) : 985 - 986
  • [50] Partial trisomy 18q due to a maternal insertion (2;18).
    Campora, L
    Zelaya, G
    Montanari, D
    Scheifer, J
    Barreiro, C
    Gallego, M
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 156 - 156
12345