Diagnosis of lethal or prenatal‐onset autosomal recessive disorders by parental exome sequencing

OBJECTIVE: Rare genetic disorders resulting in prenatal or neonatal death are genetically heterogeneous, but testing is often limited by the availability of fetal DNA, leaving couples without a potential prenatal test for future pregnancies. We describe our novel strategy of exome sequencing parenta...

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Detalles Bibliográficos
Autores principales: Stals, Karen L., Wakeling, Matthew, Baptista, Júlia, Caswell, Richard, Parrish, Andrew, Rankin, Julia, Tysoe, Carolyn, Jones, Garan, Gunning, Adam C., Lango Allen, Hana, Bradley, Lisa, Brady, Angela F., Carley, Helena, Carmichael, Jenny, Castle, Bruce, Cilliers, Deirdre, Cox, Helen, Deshpande, Charu, Dixit, Abhijit, Eason, Jacqueline, Elmslie, Frances, Fry, Andrew E., Fryer, Alan, Holder, Muriel, Homfray, Tessa, Kivuva, Emma, McKay, Victoria, Newbury‐Ecob, Ruth, Parker, Michael, Savarirayan, Ravi, Searle, Claire, Shannon, Nora, Shears, Deborah, Smithson, Sarah, Thomas, Ellen, Turnpenny, Peter D., Varghese, Vinod, Vasudevan, Pradeep, Wakeling, Emma, Baple, Emma L., Ellard, Sian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Special Topic Issue on Advances in the Diagnosis of Single Gene Disorders
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5836855/
https://www.ncbi.nlm.nih.gov/pubmed/29096039
http://dx.doi.org/10.1002/pd.5175

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5836855/
https://www.ncbi.nlm.nih.gov/pubmed/29096039
http://dx.doi.org/10.1002/pd.5175

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