TRISOMY 10Q DUE TO DENOVO DUPLICATION OF Q21 AND Q22 BANDS

被引：0
|
作者：
SURANA, RB [1 ]
PARK, MY [1 ]
机构：
[1] HOWARD UNIV,WASHINGTON,DC 20059
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 1980年 / 32卷 / 06期
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：
引用
收藏
页码：A90 / A90
页数：1
相关论文
共 50 条
  • [21] 46,XX,t(5;13)(p15;q21),t(9;21)(q22;q22),ins(14;2)(q22;q22q36)染色体异常一例
    金克勤
    徐夏苑
    饶伟强
    中华医学遗传学杂志, 2012, (05) : 619 - 619
  • [22] A t(17;20)(q21;q12) masking a variant t(15;17)(q22;q21) in a patient with acute promyelocytic leukemia
    Garcia-Casado, Zaida
    Cervera, Jose
    Valencia, Ana
    Pajuelo, Juan C.
    Mena-Duran, Armando V.
    Barragan, Eva
    Bolufer, Pascual
    Sanz, Miguel A.
    CANCER GENETICS AND CYTOGENETICS, 2006, 168 (01) : 73 - 76
  • [23] Frequent association between trisomy 15 and t(8;21)(q22;q22) in acute myeloid leukemia
    Suzuki, A
    Ohyashiki, K
    Kimura, Y
    Matsuda, S
    Sano, F
    Yamada, O
    Ohno, R
    CANCER GENETICS AND CYTOGENETICS, 2001, 126 (02) : 169 - 170
  • [24] Tetraploidy with double t(15;17)(q22;q21) in acute promyelocytic leukaemia
    Mohamed, Muhajir
    Dun, Karen
    PATHOLOGY, 2013, 45 (02) : 203 - 205
  • [25] Three's a crowd: 10q triplication secondary to a paternal 10q duplication
    Gardham, Alice
    Sullivan, Caroline
    Bernhard, Birgitta
    CLINICAL DYSMORPHOLOGY, 2014, 23 (04) : 143 - 146
  • [26] Acute myeloid leukemia (AML) with t(8;21)(q22;q22) relapsing as AML with t(3;21)(q26;q22)
    Bacher, Ulrike
    Schnittger, Susanne
    Kern, Wolfgang
    Trenn, Guido
    Weisser, Martin
    Haferlach, Torsten
    Schoch, Claudia
    CANCER GENETICS AND CYTOGENETICS, 2006, 168 (02) : 172 - 174
  • [27] PARTIAL TRISOMY 9 WITH t(9;21)(q22; q10) TRANSLOCATION DETECTED IN PRENATAL DIAGNOSIS
    Karkucak, Mutlu
    Sag, Sebnem
    Yakut, Tahsin
    Gulten, Tuna
    Gorukmez, Orhan
    Kimya, Yalcin
    TURKISH JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2012, 9 (01) : 26 - 29
  • [28] IDENTIFICATION OF A NEW CYTOGENETIC ABNORMALITY T(3 21) (Q21 Q22) IN PRIMARY MYELODYSPLASTIC SYNDROME
    SABA, HI
    NADEEM, SQ
    MOSCINSKI, LC
    SPIERS, ASD
    PAPENHAUSEN, PR
    BLOOD, 1993, 82 (10) : A556 - A556
  • [29] Fluorescence in situ hybridization identifies inversion 16 masked by t(10;16)(q24;q22), t(7;16)(q21;q22), and t(2;16)(q37;q22) in three cases of AML-M4Eo
    Reddy, KS
    Wang, S
    Montgomery, P
    Grove, W
    Robertson, LE
    CANCER GENETICS AND CYTOGENETICS, 2000, 116 (02) : 148 - 152
  • [30] SERIAL DUPLICATION OF 10 (Q21-]Q22) IN A MENTALLY-RETARDED BOY WITH CONGENITAL-MALFORMATIONS
    KOIVISTO, M
    HERVA, R
    LINNA, SL
    HUMAN GENETICS, 1981, 57 (02) : 224 - 225
12345