Prenatal diagnosis of GREIG syndrome in a fetus with a de novo translocation t(5;7)(p15;p13).

被引:0
|
作者
Morichon-Delvallez, N
Gosset, P
Delezoide, AL
Chemouny, S
Loison, S
Fert-Ferrer, S
Ozilou, C
Dumez, Y
Vekemans, M
Romana, SP
机构
[1] Hop Necker Enfants Malad, Dept Genet, Paris, France
[2] Hop Necker Enfants Malad, Prenatal Diag Ctr, Paris, France
关键词
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
1985
引用
收藏
页码:A352 / A352
页数:1
相关论文
共 50 条
  • [1] A FAMILIAL RECIPROCAL TRANSLOCATION T(3 - 7) (P21.1 - P13) ASSOCIATED WITH THE GREIG POLYSYNDACTYLY-CRANIOFACIAL ANOMALIES SYNDROME
    TOMMERUP, N
    NIELSEN, F
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1983, 16 (03): : 313 - 321
  • [2] Acute Myelogenous Leukemia with the t(7;7)(p15;p22) Translocation, a Novel Simple Variant of t(7;11)(p15;p15) Translocation: First Description
    Shibusawa, Motoharu
    CASE REPORTS IN HEMATOLOGY, 2021, 2021
  • [3] TEL rearrangements in a childhood acute leukemias associated with a t(7;12)(p15;p13).
    Wlodarska, I
    Marynen, P
    LaStarza, R
    Mecucci, C
    Uyttebroeck, A
    Verhoef, G
    VandenBerghe, H
    BLOOD, 1995, 86 (10) : 3134 - 3134
  • [4] Unusual de novo t(13;15)(q12.1;p13) translocation leading to complex mosaicism including jumping translocation
    Petit, P
    Devriendt, K
    Vermeesch, JR
    De Cock, P
    Fryns, JP
    ANNALES DE GENETIQUE, 1998, 41 (01): : 22 - 26
  • [5] GREIG SYNDROME IN A LARGE KINDRED DUE TO RECIPROCAL CHROMOSOME-TRANSLOCATION T(6,7)(Q27,P13)
    KRUGER, G
    GOTZ, J
    KVIST, U
    DUNKER, H
    ERFURTH, F
    PELZ, L
    ZECH, L
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1989, 32 (03): : 411 - 416
  • [6] Translocation (10;11)(p13;p15) in an infant acute myeloid leukemia with MLL gene rearrangement
    Marco, F
    Bureo, E
    Delgado, MD
    Richard, C
    Cuadrado, MA
    Retortillo, JAP
    Recio, M
    Zubizarreta, A
    CANCER GENETICS AND CYTOGENETICS, 1999, 114 (01) : 68 - 70
  • [7] Multiple congenital abnormalities and de novo t (3; 4) (p13; p14) translocation: Case report
    Bozaykut, Abdulkadir
    Seren, Lale Pulat
    Ipek, Ilke
    Sezer, Gonul
    Tunc, Nilufer
    MEDICAL JOURNAL OF BAKIRKOY, 2007, 3 (01) : 37 - 39
  • [8] Biallelic ETV6 rearrangements by recurrent translocations t(7;12)(p15;p13) and t(3;12)(q26.2;p13) in acute myeloid leukemia
    Yamamoto, Katsuya
    Yakushijin, Kimikazu
    Funakoshi, Yohei
    Inui, Yumiko
    Okamura, Atsuo
    Matsuoka, Hiroshi
    Minami, Hironobu
    LEUKEMIA RESEARCH, 2011, 35 (11) : E212 - E214
  • [9] Molecular cytogenetic characterization of distal 5p deletion syndrome in a fetus with a de novo aberrant chromosome 5 at prenatal diagnosis
    Chen, Chih-Ping
    TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2024, 63 (02): : 266 - 269
  • [10] Prenatal diagnosis of a de novo triplication of chromosome 9p:46,XY,trp(9)(9pter→p13::p13→p24::p24→qter)
    Smith, G
    Stewart, FJ
    Thornton, CT
    Brown, A
    JOURNAL OF MEDICAL GENETICS, 2000, 37 : S46 - S46