标题
Clinical phenotype of the recurrent 1q21.1 copy-number variant
作者
关键词
-
出版物
GENETICS IN MEDICINE
Volume 18, Issue 4, Pages 341-349
出版商
Springer Nature
发表日期
2015-06-11
DOI
10.1038/gim.2015.78
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。- Analysis of copy number variations at 15 schizophrenia-associated loci
- (2013) Elliott Rees et al. BRITISH JOURNAL OF PSYCHIATRY
- The effect of height, weight and head circumference on gross motor development in achondroplasia
- (2013) Penelope Jane Ireland et al. JOURNAL OF PAEDIATRICS AND CHILD HEALTH
- CNVs conferring risk of autism or schizophrenia affect cognition in controls
- (2013) Hreinn Stefansson et al. NATURE
- Congenital idiopathic microcephaly in an infant: Congruence of head size with developmental motor delay
- (2013) Susan R. Harris Developmental Neurorehabilitation
- Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?
- (2012) Maarten J. Van Den Bossche et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- Genome-Wide Association Study of Multiplex Schizophrenia Pedigrees
- (2012) Douglas F. Levinson et al. AMERICAN JOURNAL OF PSYCHIATRY
- Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes
- (2012) Jill A Rosenfeld et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- 1q21.1 Microduplication expression in adults
- (2012) Alessia Dolcetti et al. GENETICS IN MEDICINE
- Association testing of copy number variants in schizophrenia and autism spectrum disorders
- (2012) Bernard J Crespi et al. Journal of Neurodevelopmental Disorders
- Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts
- (2012) D Moreno-De-Luca et al. MOLECULAR PSYCHIATRY
- Simons Variation in Individuals Project (Simons VIP): A Genetics-First Approach to Studying Autism Spectrum and Related Neurodevelopmental Disorders
- (2012) The Simons VIP Consortium NEURON
- Phenotypic Heterogeneity of Genomic Disorders and Rare Copy-Number Variants
- (2012) Santhosh Girirajan et al. NEW ENGLAND JOURNAL OF MEDICINE
- Copy Number Variants in Schizophrenia: Confirmation of Five Previous Findings and New Evidence for 3q29 Microdeletions and VIPR2 Duplications
- (2011) Douglas F. Levinson et al. AMERICAN JOURNAL OF PSYCHIATRY
- An Emerging 1q21.1 Deletion-Associated Neurodevelopmental Phenotype
- (2011) Lina Basel-Vanagaite et al. JOURNAL OF CHILD NEUROLOGY
- Cognitive and Behavioral Characterization of 16p11.2 Deletion Syndrome
- (2010) Ellen Hanson et al. JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS
- The Simons Simplex Collection: A Resource for Identification of Autism Genetic Risk Factors
- (2010) Gerald D. Fischbach et al. NEURON
- Developmental Correlates of Head Circumference at Birth and Two Years in a Cohort of Extremely Low Gestational Age Newborns
- (2009) Karl C.K. Kuban et al. JOURNAL OF PEDIATRICS
- Rare chromosomal deletions and duplications increase risk of schizophrenia
- (2008) Jennifer L. Stone et al. NATURE
- Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities
- (2008) Nicola Brunetti-Pierri et al. NATURE GENETICS
- Brain morphometry with multiecho MPRAGE
- (2008) André J.W. van der Kouwe et al. NEUROIMAGE
- Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes
- (2008) Heather C. Mefford et al. NEW ENGLAND JOURNAL OF MEDICINE
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now