Further supporting evidence for theSATB2-associated syndrome found through whole exome sequencing
出版年份 2015 全文链接
标题
Further supporting evidence for theSATB2-associated syndrome found through whole exome sequencing
作者
关键词
-
出版物
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
Volume 167, Issue 5, Pages 1026-1032
出版商
Wiley
发表日期
2015-04-17
DOI
10.1002/ajmg.a.36849
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- The role of SATB2 in skeletogenesis and human disease
- (2013) Xiaoying Zhao et al. CYTOKINE & GROWTH FACTOR REVIEWS
- Further delineation of the SATB2 phenotype
- (2013) Dennis Döcker et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Disorders with similar clinical phenotypes reveal underlying genetic interaction: SATB2 acts as an activator of the UPF3B gene
- (2013) Petcharat Leoyklang et al. HUMAN GENETICS
- Disruption of SATB2 or its long-range cis-regulation by SOX9 causes a syndromic form of Pierre Robin sequence
- (2013) J. K. Rainger et al. HUMAN MOLECULAR GENETICS
- Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study
- (2012) Anita Rauch et al. LANCET
- Satb2, modularity, and the evolvability of the vertebrate jaw
- (2011) Jennifer L. Fish et al. EVOLUTION & DEVELOPMENT
- Case series: 2q33.1 microdeletion syndrome--further delineation of the phenotype
- (2011) M. Balasubramanian et al. JOURNAL OF MEDICAL GENETICS
- Roles of SATB2 in Osteogenic Differentiation and Bone Regeneration
- (2011) Jin Zhang et al. TISSUE ENGINEERING PART A
- A cross-species analysis of Satb2 expression suggests deep conservation across vertebrate lineages
- (2010) Kelly Sheehan-Rooney et al. DEVELOPMENTAL DYNAMICS
- The expression profile and function of Satb2 in zebrafish embryonic development
- (2010) Hyun-Jong Ahn et al. MOLECULES AND CELLS
- Toriello-Carey syndrome in a patient with ade novobalanced translocation [46,XY,t(2;14)(q33;q22)] interrupting SATB2
- (2009) DH Tegay et al. CLINICAL GENETICS
- 4.5 Mb microdeletion in chromosome band 2q33.1 associated with learning disability and cleft palate
- (2009) Jill Urquhart et al. European Journal of Medical Genetics
- Small Deletions of SATB2 Cause Some of the Clinical Features of the 2q33.1 Microdeletion Syndrome
- (2009) Jill A. Rosenfeld et al. PLoS One
- Satb2 Regulates Callosal Projection Neuron Identity in the Developing Cerebral Cortex
- (2008) Elizabeth A. Alcamo et al. NEURON
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