SATB2-associated syndrome presenting with Rett-like phenotypes-Reference-Cited by-同舟云学术

SATB2-associated syndrome presenting with Rett-like phenotypes

Published:2016-01-19 Issue:6 Volume:89 Page:728-732
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Lee J.S.¹,Yoo Y.²,Lim B.C.³,Kim K.J.³,Choi M.²,Chae J.-H.³

Affiliation:

1. Department of Pediatrics; Gachon University Gil Medical Center; Incheon South Korea

2. Department of Biomedical Sciences; Seoul National University College of Medicine; Seoul South Korea

3. Department of Pediatrics, Pediatric Clinical Neuroscience Center, Seoul National University Children's Hospital; Seoul National University College of Medicine; Seoul South Korea

Funder

Korea Health Industry Development Institute

Ministry for Health & Welfare, Republic of Korea

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference21 articles.

1. Identification of SATB2 as the cleft palate gene on 2q32-q33;FitzPatrick;Hum Mol Genet,2003

2. Heterozygous nonsense mutation SATB2 associated with cleft palate, osteoporosis, and cognitive defects;Leoyklang;Hum Mutat,2007

3. Further delineation of the SATB2 phenotype;Docker;Eur J Hum Genet,2014

4. Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencing;Zarate;Am J Med Genet A,2015

5. 4.5 Mb microdeletion in chromosome band 2q33.1 associated with learning disability and cleft palate;Urquhart;Eur J Med Genet,2009

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3. Genetic and Protein Network Underlying the Convergence of Rett-Syndrome-like (RTT-L) Phenotype in Neurodevelopmental Disorders;Cells;2023-05-21

4. Quantitative Phenotype Morbidity Description of SATB2-Associated Syndrome;Human Mutation;2023-04-26

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