Characteristics of 2p15-p16.1 microdeletion syndrome: Review and description of two additional patients
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Title
Characteristics of 2p15-p16.1 microdeletion syndrome: Review and description of two additional patients
Authors
Keywords
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Journal
CONGENITAL ANOMALIES
Volume 55, Issue 3, Pages 125-132
Publisher
Wiley
Online
2015-04-22
DOI
10.1111/cga.12112
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- A patient with de novo 0.45 Mb deletion of 2p16.1: The role ofBCL11A,PAPOLG,REL, andFLJ16341in the 2p15-p16.1 microdeletion syndrome
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- (2012) Vishwanathan Hucthagowder et al. European Journal of Medical Genetics
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- (2012) Marcela Raices et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
- Deletion 2p15-16.1 syndrome: Case report and review
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- The Ubiquitin-Specific Protease USP34 Regulates Axin Stability and Wnt/ -Catenin Signaling
- (2011) T. T. H. Lui et al. MOLECULAR AND CELLULAR BIOLOGY
- Haploinsufficiency of HDAC4 Causes Brachydactyly Mental Retardation Syndrome, with Brachydactyly Type E, Developmental Delays, and Behavioral Problems
- (2010) Stephen R. Williams et al. AMERICAN JOURNAL OF HUMAN GENETICS
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- Clinical and molecular characterization of two patients with overlapping de novo microdeletions in 2p14-p15 and mild mental retardation
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- A newly recognised microdeletion syndrome of 2p15-16.1 manifesting moderate developmental delay, autistic behaviour, short stature, microcephaly, and dysmorphic features: a new patient with 3.2 Mb deletion
- (2009) J-S Liang et al. JOURNAL OF MEDICAL GENETICS
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