Cardiac phenotypes in chromosome 4q− syndrome with and without a deletion of the dHAND gene
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical)
Reference23 articles.
Cited by 34 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. The Genetics of Canine Pulmonary Valve Stenosis;Veterinary Clinics of North America: Small Animal Practice;2023-11
2. Impact of genetic structural variants in factor XI deficiency: identification, accurate characterization, and inferred mechanism by long-read sequencing;Journal of Thrombosis and Haemostasis;2023-07
3. Prenatal diagnosis and molecular cytogenetic characterization of a de novo deletion of 4q34.1→qter associated with low PAPP-A and low PlGF in the first-trimester maternal serum screening, congenital heart defect on fetal ultrasound and a false negative non-invasive prenatal testing (NIPT) result;Taiwanese Journal of Obstetrics and Gynecology;2022-11
4. Clinical comparison between terminal and interstitial 4q deletion in two unrelated children;2022-10-10
5. Cytogenomic characterization of a de novo 4q34.1 deletion in a girl with mild dysmorphic features and a coagulation disorder;Molecular Cytogenetics;2021-09-04
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