Compound Heterozygosity for Novel Truncating Variants in the LMOD3 Gene as the Cause of Polyhydramnios in Two Successive Fetuses

Polyhydramnios is sometimes associated with genetic defects. However, establishing an accurate diagnosis and pinpointing the precise genetic cause of polyhydramnios in any given case represents a major challenge because it is known to occur in association with over 200 different conditions. Whole ex...

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Detalles Bibliográficos
Autores principales: Wang, Ye, Zhu, Caixia, Du, Liu, Li, Qiaoer, Lin, Mei-Fang, Férec, Claude, Cooper, David N., Chen, Jian-Min, Zhou, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753228/
https://www.ncbi.nlm.nih.gov/pubmed/31572445
http://dx.doi.org/10.3389/fgene.2019.00835

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753228/
https://www.ncbi.nlm.nih.gov/pubmed/31572445
http://dx.doi.org/10.3389/fgene.2019.00835

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