Prenatal Sonographic Features of 22q11.2 Microdeletion Syndrome
Author:
Publisher
Medknow
Subject
Radiology Nuclear Medicine and imaging
Cited by 7 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. Application of array comparative genomic hybridization on the DNA extracted from cultured amniocytes for rapid diagnosis of 22q11.2 microdeletion in a pregnancy with a normal karyotype at amniocentesis and double outlet right ventricle and transposition of great arteries on level II ultrasound;Taiwanese Journal of Obstetrics and Gynecology;2024-07
2. Isolated polyhydramnios: Is a genetic evaluation of value?;European Journal of Obstetrics & Gynecology and Reproductive Biology;2024-02
3. Central 22q11.2 deletion ( LCR22 B‐D ) in a fetus with severe fetal growth restriction and a mother with severe systemic lupus erythematosus: Further evidence of CRKL haploinsufficiency in the pathogenesis of 22q11.2 deletion syndrome;American Journal of Medical Genetics Part A;2021-07
4. Prenatal diagnosis of familial 22q11.2 deletion syndrome in a pregnancy with concomitant cardiac and urinary tract abnormalities in the fetus and the mother;Taiwanese Journal of Obstetrics and Gynecology;2021-01
5. Nomogram of Fetal Thymus Using Thy-Box Technique in South Indian Population;Journal of Fetal Medicine;2018-03-08
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