Fetal sex determination from maternal blood at 6 weeks of gestation when at risk for 21-hydroxylase deficiency
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Obstetrics and Gynaecology
Cited by 44 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. Clinical guidelines for the diagnosis and treatment of 21-hydroxylase deficiency (2021 revision);CLIN PEDIATR ENDOCRI;2022
2. Prenatal Diagnosis and Treatment in Congenital Adrenal Hyperplasia;Fertility and Reproductive Outcomes in Different Forms of Congenital Adrenal Hyperplasia;2021
3. EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency;European Journal of Human Genetics;2020-07-02
4. The Association between Placental Location in the First Trimester and Fetal Sex;Journal of Pharmaceutical Research International;2019-05-23
5. Prenatal non-invasive foetal RHD genotyping: diagnostic accuracy of a test as a guide for appropriate administration of antenatal anti-D immunoprophylaxis;BLOOD TRANSFUS-ITALY;2018
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