Related references
Note: Only part of the references are listed.KIAA1109 Variants Are Associated with a Severe Disorder of Brain Development and Arthrogryposis
Lucie Gueneau et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2018)
Whole exome sequencing as a diagnostic adjunct to clinical testing in fetuses with structural abnormalities
F. Fu et al.
ULTRASOUND IN OBSTETRICS & GYNECOLOGY (2018)
High-throughput discovery of novel developmental phenotypes
Mary E. Dickinson et al.
NATURE (2016)
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
Sue Richards et al.
GENETICS IN MEDICINE (2015)
Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families
Anas M. Alazami et al.
CELL REPORTS (2015)
Share Paper
