Annular pancreas in Trichorhinophalangeal syndrome type II with 8q23.3-q24.12 interstitial deletion

被引:0
|
作者
Qi Li
Zhen Zhang
Yuchun Yan
Ping Xiao
Zhijie Gao
Wei Cheng
Lin Su
Kaihui Yu
Hua Xie
Xiaoli Chen
Qian Jiang
Long Li
机构
[1] Capital Institute of Pediatrics,Department of Pediatric Surgery
[2] Capital Institute of Pediatrics Affiliated Children’s Hospital,2Department of Radiology
[3] Capital Institute of Pediatrics Affiliated Children’s Hospital,Department of Pathology
[4] Capital Institute of Pediatrics Affiliated Children’s Hospital,Department of Neurology
[5] Beijing United Family Hospital,Department of Surgery
[6] Monash University,Department of Paediatrics and Surgery, Faculty of Medicine, Nursing and Health Sciences
[7] Clinical College of PLA Affiliated Anhui Medical University,Reproductive Medicine Center
[8] School of Preclinical Sciences,Department of Pathophysiology
[9] Guangxi Medical University,Municipal Key Laboratory of Child Development and Nutriomics
[10] Capital Institute of Pediatrics,Department of Medical Genetics, Municipal Key Laboratory of Child Development and Nutriomics
[11] Capital Institute of Pediatrics,undefined
来源
Molecular Cytogenetics | / 8卷
关键词
Annular pancreas; 8q23.3-q24.12 deletion; Trichorhinophalangeal syndrome type II; Chinese; qPCR;
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
  • [1] Annular pancreas in Trichorhinophalangeal syndrome type II with 8q23.3-q24.12 interstitial deletion
    Li, Qi
    Zhang, Zhen
    Yan, Yuchun
    Xiao, Ping
    Gao, Zhijie
    Cheng, Wei
    Su, Lin
    Yu, Kaihui
    Xie, Hua
    Chen, Xiaoli
    Jiang, Qian
    Li, Long
    MOLECULAR CYTOGENETICS, 2015, 8
  • [2] Trichorhinophalangeal syndrome type II due to a novel 8q23.3-q24.12 deletion associated with imperforate hymen and vaginal stenosis
    Plaza-Benhumea, L.
    Valdes-Miranda, J. M.
    Toral-Lopez, J.
    Perez-Cabrera, A.
    Cuevas-Covarrubias, S.
    BRITISH JOURNAL OF DERMATOLOGY, 2014, 171 (06) : 1581 - 1583
  • [3] 8Q24.12 INTERSTITIAL DELETION IN TRICHORHINOPHALANGEAL SYNDROME TYPE-I
    FRYNS, JP
    VANDENBERGHE, H
    HUMAN GENETICS, 1986, 74 (02) : 188 - 189
  • [4] An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4
    Selenti, Nikoletta
    Tzetis, Maria
    Braoudaki, Maria
    Gianikou, Krinio
    Kitsiou-Tzeli, Sofia
    Fryssira, Helen
    MOLECULAR CYTOGENETICS, 2015, 8
  • [5] An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4
    Nikoletta Selenti
    Maria Tzetis
    Maria Braoudaki
    Krinio Giannikou
    Sofia Kitsiou-Tzeli
    Helen Fryssira
    Molecular Cytogenetics, 8
  • [6] Erratum to: An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4
    Nikoletta Selenti
    Maria Tzetis
    Maria Braoudaki
    Krinio Giannikou
    Sofia Kitsiou-Tzeli
    Helen Fryssira
    Molecular Cytogenetics, 8
  • [7] An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4 (vol 8, 64, 2015)
    Selenti, Nikoletta
    Tzetis, Maria
    Braoudaki, Maria
    Giannikou, Krinio
    Kitsiou-Tzeli, Sofia
    Fryssira, Helen
    MOLECULAR CYTOGENETICS, 2015, 8
  • [8] TRICHORHINOPHALANGEAL SYNDROME WITHOUT EXOSTOSES, WITH AN INTERSTITIAL DELETION OF 8Q23
    GOLDBLATT, J
    SMART, RD
    CLINICAL GENETICS, 1986, 29 (05) : 434 - 438
  • [9] Tibial Hemimelia in Langer-Giedion Syndrome With 8q23.1-q24.12 Interstitial Deletion
    Carvalho, Daniel Rocha
    Lima Santos, Savana Camilla
    Valverde Oliveira, Maria Dulce
    Speck-Martins, Carlos Eduardo
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2011, 155A (11) : 2784 - 2787
  • [10] Overlapping Langer Giedion Syndrome and Cornelia de Lange Syndrome type 4 an atypical case of microdeletion 8q23.3q24.12
    Plutino, Morgane
    Giuliano, Fabienne
    Dayem-Quere, Manal
    Duboc, Veronique
    Karmous-Benailly, Houda
    MOLECULAR CYTOGENETICS, 2017, 10