Clinical Conundrum: Polyhydramnios as a Marker for a Fetal Genetic Syndrome in the Canadian Old Order Mennonite Population
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology
Reference11 articles.
1. SMFM consult series #46: evaluation and management of polyhydramnios;Dashe;Am J Obstet Gynecol,2018
2. Genetic heritage of the Old Order Mennonites of southeastern Pennsylvania;Puffenberger;Am J Med Genet C Semin Med Genet,2003
3. Amish, Mennonite, and Hutterite genetic disorder database;Payne;Paediatr Child Health,2011
4. Polyhydramnios, megalencephaly and symptomatic epilepsy caused by a homozygous 7-kilobase deletion in LYK5;Puffenberger;Brain,2007
5. Abortion: review of Mennonite literature;Brenneman;Mennon Quart Rev,1979
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1. Isolated polyhydramnios: Is a genetic evaluation of value?;European Journal of Obstetrics & Gynecology and Reproductive Biology;2024-02
2. Identification of a novel intronic mutation of MAGED2 gene in a Chinese family with antenatal Bartter syndrome;BMC Medical Genomics;2024-01-18
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