Exome sequencing of fetal anomaly syndromes: novel phenotype–genotype discoveries

The monogenic etiology of most severe fetal anomaly syndromes is poorly understood. Our objective was to use exome sequencing (ES) to increase our knowledge on causal variants and novel candidate genes associated with specific fetal phenotypes. We employed ES in a cohort of 19 families with one or m...

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Detalles Bibliográficos
Autores principales: Meier, Nicole, Bruder, Elisabeth, Lapaire, Olav, Hoesli, Irene, Kang, Anjeung, Hench, Jürgen, Hoeller, Sylvia, De Geyter, Julie, Miny, Peter, Heinimann, Karl, Chaoui, Rabih, Tercanli, Sevgi, Filges, Isabel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6461982/
https://www.ncbi.nlm.nih.gov/pubmed/30679815
http://dx.doi.org/10.1038/s41431-018-0324-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6461982/
https://www.ncbi.nlm.nih.gov/pubmed/30679815
http://dx.doi.org/10.1038/s41431-018-0324-y

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