Simpson—Golabi—Behmel syndrome: Disproportionate fetal overgrowth and elevated maternal serum alpha-fetoprotein
Author:
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Reference21 articles.
1. A new X-linked dysplasia gigantism syndrome: Follow up in the first family and report on a second Austrian family
2. Hazards of hypertonic magnesium enema therapy.
3. Tissue specific control of α-fetoprotein gene expression
4. Report of another family with Simpson-Golabi-Behmel syndrome and a review of the literature
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. Prenatal diagnosis of Simpson–Golabi–Behmel syndrome type 1 with an 814 kb Xq26.2 deletion with the initial presentation of a thick nuchal fold;Taiwanese Journal of Obstetrics and Gynecology;2023-01
2. SIMPSON-GOLABI-BEHMEL syndrome type 1: How placental immunohistochemistry can rapidly Predict the diagnosis;Placenta;2022-08
3. A prenatal case of Simpson-Golabi-Behmel syndrome type 1 with a 0.26-Mb deletion fragment at Xq26.2 inherited from mother;Medicine;2022-04-22
4. Whole exome sequencing aids the diagnosis of Simpson–Golabi–Behmel syndrome in two male fetuses;Journal of International Medical Research;2019-07-15
5. Nonisolated diaphragmatic hernia in Simpson-Golabi-Behmel syndrome;Prenatal Diagnosis;2018-01
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