De novo balanced reciprocal translocation mosaic t(1;3)(q42;q25) detected by prenatal genetic diagnosis: a fetus conceived using preimplantation genetic testing due to a t(12;14)(q22;q13) balanced paternal reciprocal translocation

被引：0
|
作者：
Shaoqin Zhang
Jianjiang Zhu
Hong Qi
Limei Xu
Lirong Cai
Ran Meng
机构：
[1] Beijing Haidian Maternal and Child Health Hospital,Prenatal Diagnosis Center
来源：
Molecular Cytogenetics | / 14卷
关键词：
Pre-implantation diagnosis; PGT-SR; Prenatal diagnosis; Balanced reciprocal translocation mosaicism;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
相关论文
共 37 条
  • [31] Symmetrical upper limb peromelia and lower limb phocomelia associated with a de novo apparently balanced reciprocal translocation: 46,XX,t(2;12)(p25.1;q24.1)
    Murray, RS
    Keeling, JW
    Ellis, PM
    FitzPatrick, DR
    CLINICAL DYSMORPHOLOGY, 2002, 11 (02) : 87 - 90
  • [32] Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9) t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication
    Chen, Chih-Ping
    Lin, Chen-Ju
    Chern, Schu-Rern
    Wu, Peih-Shan
    Chen, Yen-Ni
    Chen, Shin-Wen
    Lee, Chen-Chi
    Chen, Li-Feng
    Yang, Chien-Wen
    Wang, Wayseen
    TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2016, 55 (04): : 596 - 601
  • [33] The impact of balanced reciprocal translocation - 46,XX,t(7; 17) (p13;q24) probably involving the SOX9 gene in the in vitro fertilization with own oocytes evaluated by preimplantation genetic testing or donated oocytes
    Peregrino, Pedro F. M.
    Gomes, Alecsandra
    Fujii, Mariana
    Bonetti, Tatiana C. S.
    Riboldi, Marcia
    Monteleone, Pedro A. A.
    JORNAL BRASILEIRO DE REPRODUCAO ASSISTIDA, 2019, 23 (01): : 68 - 71
  • [34] REGIONAL LOCALIZATION OF HUMAN GENES FOR MALATE DEHYDROGENASE-1 AND ISOCITRATE DEHYDROGENASE-1 ON CHROMOSOME-2 BY INTERSPECIFIC HYBRIDIZATION USING HUMAN CELLS WITH BALANCED RECIPROCAL TRANSLOCATION T(1-2) (Q32-Q13)
    FRANCKE, U
    CYTOGENETICS AND CELL GENETICS, 1975, 14 (3-6): : 308 - 312
  • [35] Cryptic 7q21 and 9p23 deletions in a patient with apparently balanced de novo reciprocal translocation t(7;9)(q21;p23) associated with a dystonia-plus syndrome:: paternal deletion of the epsilon-sarcoglycan (SGCE) gene
    Bonnet, C.
    Gregoire, M. -J.
    Vibert, M.
    Raffo, E.
    Leheup, B.
    Jonveaux, P.
    JOURNAL OF HUMAN GENETICS, 2008, 53 (10) : 876 - 885
  • [36] Cryptic 7q21 and 9p23 deletions in a patient with apparently balanced de novo reciprocal translocation t(7;9)(q21;p23) associated with a dystonia-plus syndrome: paternal deletion of the epsilon-sarcoglycan (SGCE) gene
    C. Bonnet
    M.-J. Grégoire
    M. Vibert
    E. Raffo
    B. Leheup
    P. Jonveaux
    Journal of Human Genetics, 2008, 53 : 876 - 885
  • [37] First-trimester application of expanded non-invasive prenatal testing in the genetic investigation of fetal 1p36 deletion syndrome associated with a familial unbalanced reciprocal translocation of 46,XX,der(1)t(1;2) (p36.2;q37.3)dmat
    Chen, Chih-Ping
    Weng, Shun-Long
    Wu, Fang-Tzu
    Wu, Peih-Shan
    Pan, Yen-Ting
    Chen, Wen-Lin
    Yang, Chien-Wen
    Wang, Wayseen
    TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2024, 63 (06): : 909 - 912
1234