标题
7q11.23 Duplication syndrome: Physical characteristics and natural history
作者
关键词
-
出版物
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
Volume 167, Issue 12, Pages 2916-2935
出版商
Wiley
发表日期
2015-09-03
DOI
10.1002/ajmg.a.37340
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。- Children with 7q11.23 duplication syndrome: Psychological characteristics
- (2015) Carolyn B. Mervis et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Aortopathy in the 7q11.23 microduplication syndrome
- (2014) Ashley Parrott et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Cardiovascular and genitourinary anomalies in patients with duplications within the Williams syndrome critical region: Phenotypic expansion and review of the literature
- (2014) Yuri A. Zarate et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia
- (2013) Jennifer Gladys Mulle et al. BIOLOGICAL PSYCHIATRY
- Duplication of GTF2I Results in Separation Anxiety in Mice and Humans
- (2012) Carolyn B. Mervis et al. AMERICAN JOURNAL OF HUMAN GENETICS
- 7q11.23 Microduplication: a recognizable phenotype
- (2012) A Dixit et al. CLINICAL GENETICS
- Autistic Disorder in Patients with Williams-Beuren Syndrome: A Reconsideration of the Williams-Beuren Syndrome Phenotype
- (2012) Sylvie Tordjman et al. PLoS One
- Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
- (2011) Stephan J. Sanders et al. NEURON
- Long-Term Outcomes of Patients With Cardiovascular Abnormalities and Williams Syndrome
- (2010) R. Thomas Collins et al. AMERICAN JOURNAL OF CARDIOLOGY
- Inversion of the Williams syndrome region is a common polymorphism found more frequently in parents of children with Williams syndrome
- (2010) Holly H. Hobart et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
- Incidence of diverticular disease and complicated diverticular disease in young patients with Williams syndrome
- (2010) Stefano Stagi et al. PEDIATRIC SURGERY INTERNATIONAL
- Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome
- (2009) Nathalie Van der Aa et al. European Journal of Medical Genetics
- Further clinical description of duplication of Williams–Beuren region presenting with congenital glaucoma and brachycephaly
- (2008) J.L. Merritt et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- The common inversion of the Williams–Beuren syndrome region at 7q11.23 does not cause clinical symptoms
- (2008) Elaine Tam et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Dysmorphic features, simplified gyral pattern and 7q11.23 duplication reciprocal to the Williams-Beuren deletion
- (2008) Claudia Torniero et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Clinical variability of the 22q11.2 duplication syndrome
- (2008) Christian Wentzel et al. European Journal of Medical Genetics
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