De novo Deletion of 1q31.1q32.1 in a Patient with Developmental Delay and Behavioral Disorders
Author:
Publisher
S. Karger AG
Subject
Genetics (clinical),Genetics,Molecular Biology
Reference21 articles.
1. Two cases of interstitial deletion of the long arm of chromosome 1: del(1)(q21 → q25) and del(1)(q41 → q43)
2. Interstitial deletion in the long arms of chromosome 1: 46,XY,del(1)(pter leads to q22::q25 leads to qter).
3. Molecular characterization of a patient with del(1)(q23–q25)
4. Partial monosomy or trisomy resulting from crossing over within a rearranged chromosome 1
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. A rare case of 1q31.1–q32.1 deletion with congenital heart disease;Journal of Cardiology Cases;2023-07
2. Case Report: Candidate Genes Associated With Prenatal Ultrasound Anomalies in a Fetus With Prenatally Detected 1q23.3q31.2 Deletion;Frontiers in Genetics;2021-09-23
3. Chromosome 1q31.2q32.1 deletion in an adult male with intellectual disability, dysmorphic features and obesity;Clinical Dysmorphology;2019-07
4. 1q25.2-q31.3 Deletion in a female with mental retardation, clinodactyly, minor facial anomalies but no growth retardation;Molecular Cytogenetics;2013-08-06
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