Retraction Note: Clinical characterization of familial 1p36.3 microduplication.
作者信息
Jiao Junping, Wang Yuping, Hou Yue, Gao Chao, Shi Huimin, Tian Shujuan
机构信息
Department of Neurology, The First Hospital of Hebei Medical University, Shijiangzhuang City, Hebei Province, China.
Xuanwu Hospital Capital Medical University, Beijing, China.
出版信息
Neurogenetics. 2024 Jan;25(1):49. doi: 10.1007/s10048-023-00735-7.
Abstract
摘要
相似文献
1
Retraction Note: Clinical characterization of familial 1p36.3 microduplication.撤稿说明：家族性1p36.3微重复的临床特征
Neurogenetics. 2024 Jan;25(1):49. doi: 10.1007/s10048-023-00735-7.
2
Clinical characterization of familial 1p36.3 microduplication.1p36.3 微重复家族性病例的临床特征。
Neurogenetics. 2023 Jul;24(3):201-208. doi: 10.1007/s10048-023-00722-y. Epub 2023 Jun 8.
3
Familial 1p36.3 microduplication resulting from a 1p-9q non-reciprocal translocation.由1p-9q非相互易位导致的家族性1p36.3微重复。
Eur J Med Genet. 2017 Nov;60(11):583-588. doi: 10.1016/j.ejmg.2017.08.009. Epub 2017 Aug 12.
4
Non-classical 1p36 deletion in a patient with Duane retraction syndrome: case report and literature review.一名患有杜安眼球后退综合征患者的非典型1p36缺失：病例报告及文献综述
Mol Cytogenet. 2020 Sep 7;13:42. doi: 10.1186/s13039-020-00510-5. eCollection 2020.
5
Further delineation of novel 1p36 rearrangements by array-CGH analysis: narrowing the breakpoints and clarifying the "extended" phenotype.通过阵列-CGH 分析进一步描绘新型 1p36 重排：缩小断点并阐明“扩展”表型。
Gene. 2012 Sep 15;506(2):360-8. doi: 10.1016/j.gene.2012.06.060. Epub 2012 Jul 2.
6
Cutis laxa in a patient with 1p36 deletion syndrome.1p36 缺失综合征患者的皮肤松弛症。
J Dermatol. 2018 Jul;45(7):871-873. doi: 10.1111/1346-8138.14311. Epub 2018 Apr 3.
7
Setleis syndrome due to inheritance of the 1p36.22p36.21 duplication: evidence for lack of penetrance.由于1p36.22p36.21重复遗传导致的塞特利斯综合征：外显率缺失的证据。
J Hum Genet. 2015 Nov;60(11):717-22. doi: 10.1038/jhg.2015.103. Epub 2015 Aug 27.
8
A tumor suppressor locus in familial and sporadic chordoma maps to 1p36.家族性和散发性脊索瘤中的一个肿瘤抑制基因座定位于1p36。
Int J Cancer. 2000 Jul 1;87(1):68-72.
9
Refining the Clinical Spectrum of the 17p13.3 Microduplication Syndrome: Case-Report of a Familial Small Microduplication.细化17p13.3微重复综合征的临床谱：一例家族性小微重复病例报告
Biomedicines. 2022 Nov 30;10(12):3078. doi: 10.3390/biomedicines10123078.
10
Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndrome.1p36的物理图谱、1p36单体症中断点的定位以及该综合征的临床特征
Am J Hum Genet. 2003 May;72(5):1200-12. doi: 10.1086/375179. Epub 2003 Apr 8.
本文引用的文献
1
Familial 1p36.3 microduplication resulting from a 1p-9q non-reciprocal translocation.由1p-9q非相互易位导致的家族性1p36.3微重复。
Eur J Med Genet. 2017 Nov;60(11):583-588. doi: 10.1016/j.ejmg.2017.08.009. Epub 2017 Aug 12.
Zotero 插件