Deletion of YWHAE in a patient with periventricular heterotopias and pronounced corpus callosum hypoplasia
Author:
Publisher
BMJ
Subject
Genetics (clinical),Genetics
Cited by 36 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. YWHAE loss of function causes a rare neurodevelopmental disease with brain abnormalities in human and mouse;Genetics in Medicine;2023-07
2. Clinical findings and genetic analysis of patients with copy number variants involving 17p13.3 using a single nucleotide polymorphism array: a single-center experience;BMC Medical Genomics;2022-12-21
3. Further expansion and confirmation of phenotype in rare loss of YWHAE gene distinct from Miller–Dieker syndrome;American Journal of Medical Genetics Part A;2022-11-25
4. The Effect of Radiofrequency Waves on Pregnant Mice in Association with Genes Involved in Neuronal Migration;Journal of Clinical Obstetrics & Gynecology;2022
5. Prenatal Diagnosis of 17p11.2 Copy Number Abnormalities Associated With Smith–Magenis and Potocki–Lupski Syndromes in Fetuses;Frontiers in Genetics;2021-12-21
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