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
  • [1] ISOCHROMOSOME 18Q WITH KARYOTYPE-46,XX,I(18Q) - CYTOGENETICS AND PATHOLOGY
    FROSTERISKENIUS, U
    COERDT, W
    REHDER, H
    SCHWINGER, E
    CLINICAL GENETICS, 1984, 26 (06) : 549 - 554
  • [2] Prenatal diagnosis of i(18q) and dup(18q) cases by Quantitative Fluorescent Polymerase Chain Reaction
    Castro-Volio, Isabel
    Ortiz-Montero, Fernando
    Valle-Bourrouet, Luisa
    Malespin-Bendana, Wendy
    CHROMOSOME RESEARCH, 2013, 21 : S61 - S61
  • [3] AN AUTOPSIED CASE WITH 46,XX,I(18Q)
    AKAMATSU, Y
    ANDO, G
    IESHIMA, A
    TAKADA, K
    TAKASHIMA, S
    TAKESHITA, K
    TERATOLOGY, 1982, 26 (01) : A40 - A40
  • [4] Cytogenetic investigation of a child with a mosaic isochromosome 18q and ring 18q
    Souraty, Noeelle
    Sanlaville, Damien
    Chedid, Rima
    Le Lorc'h, Marc
    Maurin, Marie-Laure
    Ghanem, Lola
    Maalouf, Sabine
    Vekemans, Michel
    Wegarbane, Andre
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2007, 50 (05) : 379 - 385
  • [5] HOLOPROSENCEPHALY IN A NEWBORN GIRL WITH 46,XX,I(18Q)
    SPINNER, NB
    EUNPU, DL
    AUSTRIA, JR
    MAMUNES, P
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1991, 39 (01): : 11 - 12
  • [6] ISOCHROMOSOME (18Q) IN SIBLINGS
    KRUGER, G
    GOTZ, J
    DUNKER, H
    PELZ, L
    CLINICAL GENETICS, 1987, 32 (04) : 249 - 253
  • [7] Isochromosome 18q revisited
    Park, JP
    Moeschler, JB
    PRENATAL DIAGNOSIS, 1997, 17 (06) : 589 - 590
  • [8] DUPLICATION 18Q SYNDROME
    EHRLICH, S
    BUSTOS, T
    PAIKA, IJ
    MILUNSKY, A
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1983, 15 (02): : 261 - 263
  • [9] 46,XY,i(18q)一例报告
    齐瑛
    遗传与疾病, 1991, (04) : 247 - 247
  • [10] No evidence for imprinting in distal 18q
    Maiwald, R
    Overhauser, J
    Laccone, F
    JOURNAL OF MEDICAL GENETICS, 2000, 37 (02) : 152 - 156
12345