LETHAL OSTEOGENESIS IMPERFECTA ASSOCIATED WITH 46,XY,INV(7)(P13Q22) KARYOTYPE

被引：2
|
作者：
KNISELY, AS
RICHARDSON, A
ABUELO, D
CASEY, S
SINGER, DB
机构：
[1] BROWN UNIV,DIV BIOL & MED,PROGRAM DEV PATHOL,PROVIDENCE,RI 02912
[2] RHODE ISL HOSP,DEPT PEDIAT,PROVIDENCE,RI 02905
来源：
JOURNAL OF MEDICAL GENETICS | 1988年 / 25卷 / 05期
关键词：
D O I：
10.1136/jmg.25.5.352
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：352 / 355
页数：4
相关论文
共 50 条
  • [1] 46,XY,der(7)inv(7)(pterp13)t(1；7)(p34.3；p13)inv(7)(p13q22)一例
    李琳琳
    王瑞雪
    李磊磊
    朱海波
    胡孝南
    刘睿智
    张红国
    中华医学遗传学杂志, 2019, (07) : 751 - 751
  • [2] ACUTE MYELOMONOCYTIC LEUKEMIA WITH INV(16)(P13Q22) IN AN XY/XYY MALE
    OHYASHIKI, JH
    OHYASHIKI, K
    IWABUCHI, H
    LIN, KY
    TOYAMA, K
    CANCER GENETICS AND CYTOGENETICS, 1987, 29 (02) : 331 - 332
  • [3] HYPOPLASTIC ACUTE-LEUKEMIA ASSOCIATED WITH INV(16)(P13Q22)
    NAKAMURA, H
    MAEDA, T
    KOHNO, T
    SADAMORI, N
    ICHIMARU, M
    CANCER GENETICS AND CYTOGENETICS, 1991, 51 (01) : 63 - 66
  • [4] FISH analysis of selected secondary karyotype abnormalities in acute myeloid leukemias with an inv(16)(p13q22)
    Pirc-Danoewinata, H
    König, M
    Mitterbauer, M
    Nowotny, H
    Jäger, U
    Haas, OA
    CYTOGENETICS AND CELL GENETICS, 1999, 85 (1-2): : 83 - 83
  • [5] 46,XY,inv(7)(p22q34)一例
    邹朋书
    牟凯
    张金艳
    曹东华
    中华医学遗传学杂志, 2014, 31 (03) : 413 - 413
  • [6] A case with a cytogenetically cryptic variant of the inv(16)(p13q22)/t(16;16)(p13;q22)
    Van Obbergh, Florence
    Michaux, Lucienne
    Maertens, Johan
    Schoemans, Helene
    Vandenberghe, Peter
    CANCER GENETICS, 2014, 207 (05) : 231 - 232
  • [7] Clustering of genomic inv(16)(p13q22) breakpoints in acute nonlymphocytic leukemia
    vanderReijden, BA
    Wijmenga, C
    Liu, P
    Dauwerse, JG
    Giles, RH
    Changur, S
    vanOmmen, GJ
    Hagemeijer, A
    Breuning, M
    BLOOD, 1995, 86 (10) : 2968 - 2968
  • [8] Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered
    van der Reijden, BA
    Dauwerse, HG
    Giles, RH
    Jagmohan-Changur, S
    Wijmenga, C
    Liu, PP
    Smit, B
    Wessels, HW
    Beverstock, GC
    Jotterand-Bellomo, M
    Martinet, D
    Mühlematter, D
    Lafage-Pochitaloff, M
    Gabert, J
    Reiffers, J
    Bilhou-Nabera, C
    van Ommen, GJB
    Hagemeijer, A
    Breuning, MH
    ONCOGENE, 1999, 18 (02) : 543 - 550
  • [9] Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered
    Bert A van der Reijden
    Hans G Dauwerse
    Rachel H Giles
    Shantie Jagmohan-Changur
    Cisca Wijmenga
    P Paul Liu
    Bep Smit
    Hans W Wessels
    Geoff C Beverstock
    Martine Jotterand-Bellomo
    Danielle Martinet
    Dominique Mühlematter
    Marina Lafage-Pochitaloff
    Jean Gabert
    Josy Reiffers
    Chrystèle Bilhou-Nabera
    Gert-Jan B van Ommen
    Anne Hagemeijer
    Martijn H Breuning
    Oncogene, 1999, 18 : 543 - 550
  • [10] The prognostic significance of 3′ CBFB deletions in inv(16)(p13q22)/t(16;16)(p13;q22)
    Huxley, E
    Griffiths, MJ
    Talley, P
    Whitworth, A
    Humphreys, M
    McKinley, M
    JOURNAL OF MEDICAL GENETICS, 2005, 42 : S81 - S81
12345