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
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
  • [21] Retinoblastoma in a Case of 18q Deletion Syndrome
    Yoshida, Kaoru
    Terashima, Keita
    Yoshida, Masanori
    Nakabayashi, Kazuhiko
    Shirai, Ryota
    Yoshioka, Takako
    Nishina, Sachiko
    Azuma, Noriyuki
    Hata, Kenichiro
    Kato, Motohiro
    PEDIATRIC BLOOD & CANCER, 2020, 67
  • [22] TRISOMY 18Q - TRISOMY MAPPING OF CHROMOSOME 18 REVISITED
    TURLEAU, C
    CHAVINCOLIN, F
    NARBOUTON, R
    ASENSI, D
    DEGROUCHY, J
    CLINICAL GENETICS, 1980, 18 (01) : 20 - 26
  • [23] A patient with hypopituitarism and isochromosome 18q mosaicism
    Turan, S
    Saka, N
    Guney, I
    Bereket, A
    HORMONE RESEARCH, 2005, 64 (06) : 261 - 265
  • [24] Duplication of 18q without phenotypic effect
    Evans, C
    Rooney, DE
    Shears, DJ
    Garrett, C
    JOURNAL OF MEDICAL GENETICS, 2003, 40 : S59 - S59
  • [25] Autoimmune thyroiditis in 18Q deletion syndrome
    Lomenick, JP
    Smith, WJ
    Rose, SR
    JOURNAL OF PEDIATRICS, 2005, 147 (04): : 541 - 543
  • [26] Mosaic Isochromosome 18q: case - report
    Munoz F, Maria Paz
    Avendano B, Isabel
    Aracena A, Mariana
    Guerrero C, Tm Ximena
    REVISTA CHILENA DE PEDIATRIA-CHILE, 2009, 80 (02): : 157 - 160
  • [27] PRENATAL MORPHOLOGY OF PARTIAL MONOSOMY 18Q
    LAZJUK, G
    ZOLOTUKHINA, T
    KIRILLOVA, I
    LURIE, I
    NOVIKOVA, I
    ABASHEVA, G
    ZENTRALBLATT FUR GYNAKOLOGIE, 1987, 109 (02): : 126 - 129
  • [28] Hearing impairment in 18q deletion syndrome
    Jayarajan, V
    Swan, IRC
    Patton, MA
    JOURNAL OF LARYNGOLOGY AND OTOLOGY, 2000, 114 (12): : 963 - 966
  • [29] PRENATAL-DIAGNOSIS OF 46,XX,I(18Q) ASSOCIATED WITH HOLOPROSENCEPHALY AND CYCLOPIA
    FERRE, MM
    KEENE, CL
    JEWELL, AJ
    STETKA, DG
    AMERICAN JOURNAL OF HUMAN GENETICS, 1993, 53 (03) : 1568 - 1568
  • [30] Molecular and Clinical Characterization of a Recurrent Cryptic Unbalanced t(4q;18q) Resulting in an 18q Deletion and 4q Duplication
    Horbinski, Craig
    Carter, Erika M.
    Heard, Patricia L.
    Sathanoori, Malini
    Hu, Jie
    Vockley, Jerry
    Gunn, Shelly
    Hale, Daniel E.
    Surti, Urvashi
    Cody, Jannine D.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2008, 146A (22) : 2898 - 2904