Pages that link to "Q89587667"

The following pages link to Arthur L Beaudet (Q89587667):

Displaying 15 items.

• Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size (Q29544005) (← links)
• Homozygous and hemizygous CNV detection from exome sequencing data in a Mendelian disease cohort (Q31149204) (← links)
• Rare DNA copy number variants in cardiovascular malformations with extracardiac abnormalities (Q36543066) (← links)
• TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities (Q37083438) (← links)
• Lessons learned from additional research analyses of unsolved clinical exome cases (Q37715741) (← links)
• Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium. (Q40145504) (← links)
• A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction. (Q42375961) (← links)
• Corrigendum: High-throughput discovery of novel developmental phenotypes. (Q49965968) (← links)
• Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical Management. (Q50260153) (← links)
• Reliable detection of subchromosomal deletions and duplications using cell-based noninvasive prenatal testing (Q57788830) (← links)
• Identification of genes required for eye development by high-throughput screening of mouse knockouts (Q60300295) (← links)
• Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts (Q64120095) (← links)
• Human and mouse essentiality screens as a resource for disease gene discovery (Q89474376) (← links)
• The Deep Genome Project (Q89488064) (← links)
• Obituary: Laird Jackson (Q89587669) (← links)