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List of works by Saeed H Al Turki

Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect.

scientific article published on 21 May 2015

Improving hearing loss gene testing: a systematic review of gene evidence toward more efficient next-generation sequencing-based diagnostic testing and interpretation.

scientific article

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.

scientific article published in July 2014

Using large sequencing data sets to refine intragenic disease regions and prioritize clinical variant interpretation.

scientific article

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