Further supporting evidence for theSATB2-associated syndrome found through whole exome sequencing-Reference-Cited by-同舟云学术

Further supporting evidence for theSATB2-associated syndrome found through whole exome sequencing

Published:2015-04-17 Issue:5 Volume:167 Page:1026-1032
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Zarate Yuri A.¹,Perry Hazel²,Ben-Omran Tawfeg³,Sellars Elizabeth A.¹,Stein Quinn⁴,Almureikhi Mariam³,Simmons Kirk⁵,Klein Ophir²,Fish Jennifer⁶,Feingold Murray⁷,Douglas Jessica⁷,Kruer Michael C.⁴,Si Yue⁸,Mao Rong⁸,McKnight Dianalee⁹,Gibellini Federica⁹,Retterer Kyle⁹,Slavotinek Anne¹⁰

Affiliation:

1. Section of Genetics and Metabolism; University of Arkansas for Medical Sciences; Little Rock Arkansas

2. Division of Craniofacial Anomalies; University of California San Francisco Department of Orofacial Sciences; San Francisco California

3. Clinical and Metabolic Genetics; Department of Pediatrics; Hamad Medical Corporation Doha Qatar

4. Divisions of Pediatric Neurology & Genetics; Sanford Children's Specialty Clinic; Sanford Children's Hospital; Sioux Falls South Dakota

5. Deparment of Dentistry; University of Arkansas for Medical Sciences; Little Rock Arkansas

6. Department of Orthopaedic Surgery; University of California San Francisco; San Francisco California

7. Division of Genetics and Genomics; Feingold Center; Boston Children's Hospital; Boston Massachusetts

8. Molecular Genetics and Genomics; ARUP Laboratories; Salt Lake City Utah

9. GeneDx; Gaithersburg Maryland

10. Division of Genetics; Department of Pediatrics; University of California San Francisco; San Francisco California

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36849/fullpdf

Reference20 articles.

1. The expression profile and function of Satb2 in zebrafish embryonic development;Ahn;Mol Cells,2010

2. Satb2 regulates callosal projection neuron identity in the developing cerebral cortex;Alcamo;Neuron,2008

3. Case series: 2q33.1 microdeletion syndrome-further delineation of the phenotype;Balasubramanian;J Med Genet,2011

4. Novel transcription factor Satb2 interacts with matrix attachment region DNA elements in a tissue-specific manner and demonstrates cell-type-dependent expression in the developing mouse CNS;Britanova;Eur J Neurosci,2005

5. Satb2 haploinsufficiency phenocopies 2q32-q33 deletions, whereas loss suggests a fundamental role in the coordination of jaw development;Britanova;Am J Hum Genet,2006

Cited by 44 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Glass syndrome derived from chromosomal breakage downstream region of SATB2;Brain and Development;2024-10

2. Semaphorin heterodimerization in cis regulates membrane targeting and neocortical wiring;Nature Communications;2024-08-16

3. Progress of epigenetic modification of SATB2 gene in the pathogenesis of non-syndromic cleft lip and palate;Asian Journal of Surgery;2024-01

4. SATB2-associated syndrome: a case report;Journal of Oral Medicine and Oral Surgery;2024

5. Genetic analysis of a child with SATB2‑associated syndrome and literature study;Experimental and Therapeutic Medicine;2023-06-20