Cargando…

Copy number variation analysis in Chinese children with complete atrioventricular canal and single ventricle

BACKGROUND: Congenital heart disease (CHD) is one of the most common birth defects. Copy number variations (CNVs) have been proved to be important genetic factors that contribute to CHD. Here we screened genome-wide CNVs in Chinese children with complete atrioventricular canal (CAVC) and single vent...

Descripción completa

Detalles Bibliográficos
Autores principales:	Zhang, Xingyu, Wang, Bo, You, Guoling, Xiang, Ying, Fu, Qihua, Yu, Yongguo, Zhang, Xiaoqing
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2021
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8502261/ https://www.ncbi.nlm.nih.gov/pubmed/34627233 http://dx.doi.org/10.1186/s12920-021-01090-y

Ejemplares similares

Complete atrioventricular canal
por: Calabrò, Raffaele, et al.
Publicado: (2006)

Copy number variation-associated lncRNAs may contribute to the etiologies of congenital heart disease
por: Lu, Yibo, et al.
Publicado: (2023)

Rare Copy Number Variations in a Chinese Cohort of Autism Spectrum Disorder
por: Fan, Yanjie, et al.
Publicado: (2018)

Contribution of Copy Number Variation to Down Syndrome-associated Atrioventricular Septal Defects
por: Ramachandran, Dhanya, et al.
Publicado: (2014)

Integrated analysis of copy number variation-associated lncRNAs identifies candidates contributing to the etiologies of congenital kidney anomalies
por: Lu, Yibo, et al.
Publicado: (2023)

Rare copy number variation analysis identifies disease-related variants in atrioventricular septal defect patients
por: Hu, Huan, et al.
Publicado: (2023)

Rare Occurrence of Absent Pulmonary Valve Syndrome in the Setting of Double-Outlet Right Ventricle with Unbalanced Complete Atrioventricular Canal Defect
por: Parikh, Kinjal, et al.
Publicado: (2019)

Detection of copy number variations and their effects in Chinese bulls
por: Zhang, Liangzhi, et al.
Publicado: (2014)

A Map of Copy Number Variations in Chinese Populations
por: Lou, Haiyi, et al.
Publicado: (2011)

Anaesthetic management of a child with unrepaired complete atrioventricular canal defect, double outlet ventricle and pulmonary stenosis for non-cardiac surgery
por: Kerai, Sukhyanti, et al.
Publicado: (2022)

Copy number variations in 119 Chinese children with idiopathic short stature identified by the custom genome-wide microarray
por: Hu, Guorui, et al.
Publicado: (2016)

Genome-Wide Identification of Copy Number Variations in Chinese Holstein
por: Jiang, Li, et al.
Publicado: (2012)

ATRIOVENTRICULAR CANAL DEFECT
Publicado: (1977)

A Novel Multiplex HRM Assay to Detect Clopidogrel Resistance
por: Zhang, Lichen, et al.
Publicado: (2017)

Novel dominant-negative FOXJ1 mutation in a family with heterotaxy plus mouse model
por: Li, Lulu, et al.
Publicado: (2023)

A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease
por: Zhang, Xiaoqing, et al.
Publicado: (2015)

Rare Copy Number Variants in Isolated Sporadic and Syndromic Atrioventricular Septal Defects
por: Priest, James R, et al.
Publicado: (2012)

Retrospective Study of Complete Atrioventricular Canal Defects: Anesthetic and Perioperative Challenges
por: Janai, Aniruddha Ramesh, et al.
Publicado: (2018)

A case of a complete atrioventricular canal defect in a ferret
por: Agudelo, Carlos F, et al.
Publicado: (2021)

Genome-wide patterns of copy number variation in the Chinese yak genome
por: Zhang, Xiao, et al.
Publicado: (2016)

Genetics of atrioventricular canal defects
por: Pugnaloni, Flaminia, et al.
Publicado: (2020)

Analysis of copy number variations and possible candidate genes in spontaneous abortion by copy number variation sequencing
por: Bai, Wei, et al.
Publicado: (2023)

Copy number variations among silkworms
por: Zhao, Qian, et al.
Publicado: (2014)

Copy number variations and cancer
por: Shlien, Adam, et al.
Publicado: (2009)

Copy number variations and stroke
por: Colaianni, Valeria, et al.
Publicado: (2016)

Copy Number Variations and Schizophrenia
por: Szecówka, Kamila, et al.
Publicado: (2022)

Copy Number Variation and Osteoporosis
por: Lovšin, Nika
Publicado: (2023)

Copy number variation in Han Chinese individuals with autism spectrum disorder
por: Gazzellone, Matthew J, et al.
Publicado: (2014)

Copy-number-variation and copy-number-alteration region detection by cumulative plots
por: Li, Wentian, et al.
Publicado: (2009)

Copy number variations associated with fetal congenital kidney malformations
por: Cai, Meiying, et al.
Publicado: (2020)

Anesthetic management of a child with complete atrioventricular septal defect and single ventricle posted for noncardiac surgery
por: Mir, Aabid Hussain, et al.
Publicado: (2016)

Complete Atrioventricular Canal Defect in a Non-syndromic Adult Patient: An Unusual Presentation
por: Nabhan, Elias M, et al.
Publicado: (2023)

Transcatheter Edge-to-Edge Repair for Left Atrioventricular Valve Cleft After Previously Repaired Complete Atrioventricular Canal Defect in Down Syndrome
por: Mital, Rohit, et al.
Publicado: (2022)

New Copy Number Variations in Schizophrenia
por: Magri, Chiara, et al.
Publicado: (2010)

Copy number variation in African Americans
por: McElroy, Joseph P, et al.
Publicado: (2009)

Copy number variation goes clinical
por: Le Caignec, Cédric, et al.
Publicado: (2009)

Copy number variation in Parkinson's disease
por: Toft, Mathias, et al.
Publicado: (2010)

Copy number variation in the bovine genome
por: Fadista, João, et al.
Publicado: (2010)

Copy Number Variation in Thai Population
por: Suktitipat, Bhoom, et al.
Publicado: (2014)

Copy Number Variation in the Horse Genome
por: Ghosh, Sharmila, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_tbs0reu74tutv5cof85vv9p345