de novo interstitial deletions at the 11q23.3-q24.2 region

被引：0
作者：
Jiasun Su
Rongyu Chen
Jingsi Luo
Xin Fan
Chunyun Fu
Jin Wang
Sheng He
Xuyun Hu
ShuJie Zhang
Shang Yi
Shaoke Chen
Yiping Shen
机构：
[1] Guangxi Maternal and Child Health Hospital,Department of Genetic and Metabolic Central Laboratory
[2] Boston Children’s Hospital,Department of Laboratory Medicine
来源：
Molecular Cytogenetics | / 9卷
关键词：
Jacobsen syndrome; Contiguous gene deletion syndrome; Chromosomal microarray; Interstitial deletion;
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 50 条
  • [31] Association of Jacobsen syndrome and bipolar affective disorder in a patient with a de Novo 11q terminal deletion
    Böhm, D
    Hoffmann, K
    Laccone, F
    Wilken, B
    Dechent, P
    Frahm, J
    Bartels, I
    Bohlander, SK
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2006, 140A (04) : 378 - 382
  • [32] Girl with combined cellular immunodeficiency, pancytopenia, malformations, deletion 11q23.3→qter, and trisomy 8q24.3→qter
    Ounap, K
    Bartsch, O
    Uibo, O
    Laidre, P
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 108 (04): : 322 - 326
  • [33] Unbalanced translocations of 20q in AML and MDS often involve interstitial rather than terminal deletions of 20q
    MacKinnon, Ruth N.
    Duivenvoorden, Hendrika M.
    Campbell, Lynda J.
    [J]. CANCER GENETICS, 2011, 204 (03) : 153 - 161
  • [34] Case report: A new de novo 6q21q22.1 interstitial deletion case in a girl with cerebellar vermis hypoplasia and developmental delay and literature review
    Minotti, Chiara
    Graziani, Ludovico
    Sallicandro, Ester
    Digilio, Maria Cristina
    Falasca, Roberto
    Alesi, Viola
    Novelli, Giuseppe
    Dentici, Maria Lisa
    Loddo, Sara
    Novelli, Antonio
    [J]. FRONTIERS IN GENETICS, 2024, 14
  • [35] De Novo Interstitial Deletion of 1q32.2-q32.3 Including the Entire IRF6 Gene in a Patient with Oral Cleft and Other Dysmorphic Features
    Salahshourifar, I.
    Halim, A. S.
    Sulaiman, W. A. W.
    Ariffin, R.
    Nor, N. Naili Muhamad
    Zilfalil, B. A.
    [J]. CYTOGENETIC AND GENOME RESEARCH, 2011, 134 (02) : 83 - 87
  • [36] De novo Deletion of 1q31.1-q32.1 in a Patient with Developmental Delay and Behavioral Disorders
    Milani, D.
    Bedeschi, M. F.
    Iascone, M.
    Chiarelli, G.
    Cerutti, M.
    Menni, F.
    [J]. CYTOGENETIC AND GENOME RESEARCH, 2012, 136 (03) : 167 - 170
  • [37] Interstitial deletion 11q - Case report and review of the literature
    De Pater, JM
    Ippel, PF
    Bijlsma, JB
    Van Nieuwenhuizen, O
    [J]. GENETIC COUNSELING, 1997, 8 (04): : 335 - 339
  • [38] 11q24.2-25 Micro-Rearrangements in Autism Spectrum Disorders: Relation to Brain Structures
    Maruani, Anna
    Huguet, Guillaume
    Beggiato, Anita
    ElMaleh, Monique
    Toro, Roberto
    Leblond, Claire S.
    Mathieu, Alexandre
    Amsellem, Frederique
    Lemiere, Nathalie
    Verloes, Alain
    Leboyer, Marion
    Gillberg, Christopher
    Bourgeron, Thomas
    Delorme, Richard
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2015, 167 (12) : 3019 - 3030
  • [39] Interstitial 11q Deletion Derived From a Maternal ins(4;11)(p14;q24-2q25): A Patient Report and Review
    van Zutven, Laura J. C. M.
    van Bever, Yolande
    van Nieuwland, Carolien C. M.
    Huijbregts, Gido C. M.
    Van Opstal, Diane
    von Bergh, Anne R. M.
    Corel, Linda J. A.
    Tibboel, Dick
    Wouters, Cokkie H.
    Poddighe, Pino J.
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2009, 149A (07) : 1468 - 1475
  • [40] Prenatal diagnosis in a fetus with de-novo 20q11.2q13.1 deletion and review of the literature
    Turgal, Mert
    Ozyuncu, Ozgur
    Utine, G. Eda
    Kilic, Esra
    Boduroglu, Koray
    [J]. CLINICAL DYSMORPHOLOGY, 2014, 23 (03) : 111 - 113
12345