Similar Items: Three Unrelated Children With Childhood Apraxia of Speech: Exome Sequencing and Functional Gene Analysis Imply a Role of Laminin-511 in Early Neurodevelopment
- Prenatal Etiology Diagnosis of Rare Compound Heterozygous PROC Gene Variants in a Fetus With Ocular Ultrasonic Anomaly Using Whole Exome Sequencing
- Whole exome sequencing: a customised approach to exploring the genetic basis of musculoskeletal soft tissue injuries
- Genetic aetiology of autosomal recessive non-syndromic hearing loss in sub-Saharan African patients: evaluation using targeted and whole exome sequencing
- Whole exome sequencing to investigate genetic variants of non-syndromic hearing impairment in a population of African ancestry
- Childhood apraxia of speech: concept, diagnosis and intervention techniques
- Full-length transcriptome sequencing and identification of skin colour-associated genes in red tilapia