Implications of COMT long-range interactions on the phenotypic variability of 22q11.2 deletion syndrome
出版年份 2013 全文链接
标题
Implications of COMT long-range interactions on the phenotypic variability of 22q11.2 deletion syndrome
作者
关键词
-
出版物
Nucleus
Volume 4, Issue 6, Pages 487-493
出版商
Informa UK Limited
发表日期
2013-12-06
DOI
10.4161/nucl.27364
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes
- (2013) Maria Delio et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Genome-wide Chromatin Interactions of the Nanog Locus in Pluripotency, Differentiation, and Reprogramming
- (2013) Effie Apostolou et al. Cell Stem Cell
- Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis
- (2013) LANCET
- Genomic Interaction Profiles in Breast Cancer Reveal Altered Chromatin Architecture
- (2013) Michael J. Zeitz et al. PLoS One
- Transgene- and locus-dependent imprinting reveals allele-specific chromosome conformations
- (2013) N. Lonfat et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Phenotypic variability of atypical 22q11.2 deletions not includingTBX1
- (2012) Judith M.A. Verhagen et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Overt cleft palate phenotype andTBX1genotype correlations in velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients
- (2012) Sean B. Herman et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Heart defects and other features of the 22q11 distal deletion syndrome
- (2012) Christina R. Fagerberg et al. European Journal of Medical Genetics
- Determining long-range chromatin interactions for selected genomic sites using 4C-seq technology: From fixation to computation
- (2012) Erik Splinter et al. METHODS
- The long-range interaction landscape of gene promoters
- (2012) Amartya Sanyal et al. NATURE
- Dysregulation of DGCR6 and DGCR6L: psychopathological outcomes in chromosome 22q11.2 deletion syndrome
- (2012) D Chakraborty et al. Translational Psychiatry
- Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/digeorge/22q11.2 deletion syndrome patients
- (2011) Tingwei Guo et al. HUMAN MUTATION
- Mapping and analysis of chromatin state dynamics in nine human cell types
- (2011) Jason Ernst et al. NATURE
- An oestrogen-receptor-α-bound human chromatin interactome
- (2009) Melissa J. Fullwood et al. NATURE
- 22q11.2 Distal Deletion: A Recurrent Genomic Disorder Distinct from DiGeorge Syndrome and Velocardiofacial Syndrome
- (2008) Shay Ben-Shachar et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Velo-cardio-facial syndrome: 30 Years of study
- (2008) Robert J. Shprintzen Developmental Disabilities Research Reviews
- Deletion of ERK2 Mitogen-Activated Protein Kinase Identifies Its Key Roles in Cortical Neurogenesis and Cognitive Function
- (2008) I. S. Samuels et al. JOURNAL OF NEUROSCIENCE
- Strong association of de novo copy number mutations with sporadic schizophrenia
- (2008) Bin Xu et al. NATURE GENETICS
- Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes
- (2008) Heather C. Mefford et al. NEW ENGLAND JOURNAL OF MEDICINE
- Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication
- (2008) Blake C Ballif et al. Molecular Cytogenetics
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