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
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology
Reference16 articles.
1. A previously unrecognized X-linked syndrome of dysmorphia;Simpson;Birth Defects Orig Artic Ser,1975
2. Simpson-Golabi-Behmel syndrome types I and II;Tenorio;Orphanet J Rare Dis,2014
3. Two consecutive pregnancies with simpson-golabi-behmel syndrome type 1: case report and review of published prenatal cases;Ridnõi;Molecular syndromology,2018
4. Simpson-Golabi-Behmel syndrome: disproportionate fetal overgrowth and elevated maternal serum alpha-fetoprotein;Hughes-Benzie;Prenat Diagn,1994
5. Infantile lethal variant of Simpson-Golabi-Behmel syndrome associated with hydrops fetalis;Terespolsky;Am J Med Genet,1995
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