Identification of modifiers of 22q11.2 deletion syndrome in whole genome sequence â CIDR

NIAID Data Ecosystem2026-05-02 收录

22q11.2缺失综合征

遗传修饰因子识别

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https://www.ncbi.nlm.nih.gov/sra/SRP506951 数据链接链接失效反馈

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Identification of modifiers of 22q11.2 deletion syndrome in whole genome sequence _ CIDR

创建时间：

2024-06-06

Congenital Heart Disease Revealing Familial 22q11 Deletion Syndrome

先天性心脏病

22q11.2缺失综合征

Abstract Congenital heart defects are the most common birth defects and the leading cause of mortality in the first year of life. It is well known that the 22q11 deletion syndrome (22q11DS) is the mos

DataCite Commons2020-08-26 更新120

Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia

精神分裂症遗传易感性

22q11.2缺失综合征

The location of a schizophrenia susceptibility locus at chromosome 22q11 has been suggested by genome-wide linkage studies. Additional support was provided by the observation of a higher-than-expected

PubMed Central2002-03-12 更新40

Whole Genome Sequencing of Two Family Trios with 22q.11.2 Deletion Syndrome

22q11.2缺失综合征

遗传修饰因子识别

Two subjects with 22q11.2 deletion syndromes (22q11DS) and their parents were recruited for a whole genome sequencing study to identify candidate genetic modifiers of the various phenotypes seen in 22

NIAID Data Ecosystem30

Evaluation of an online mindfulness training for adolescents with 22q11.2 Deletion Syndrome

22q11.2缺失综合征

正念干预

The goal of this study was to evaluate the effectiveness of the Aware Program, an online mindfulness education program, with adolescents (aged 12-19 years) with 22q11.2 Deletion Syndrome and one of th

DataCite Commons2024-11-29 更新50

DataSheet_1_Association Between Parental Anxiety and Depression Level and Psychopathological Symptoms in Offspring With 22q11.2 Deletion Syndrome.docx

22q11.2缺失综合征

跨代心理病理关联

22q11.2 deletion syndrome (22q11DS) is recognized as one of the strongest genetic risk factors for the development of psychopathology, including dramatically increased prevalence of schizophrenia anxi

NIAID Data Ecosystem30

Identification of modifiers of 22q11.2 deletion syndrome in whole genome sequence â CIDR

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Identification of modifiers of 22q11.2 deletion syndrome in whole genome sequence â CIDR