Related Experiment Videos
Carrier detection and genetic counselling in Duchenne dystrophy
Developmental Medicine and Child Neurology
|June 1, 1975
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Mutations in MYH7 cause Multi-minicore Disease (MmD) with variable cardiac involvement.
Neuromuscular disorders : NMD·2012
Remission of clinical signs in early duchenne muscular dystrophy on intermittent low-dosage prednisolone therapy.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society·2002
Neonatal arthrogryposis and absent limb muscles: a muscle developmental gene defect?
Neuromuscular disorders : NMD·2001
HABIT-ILE in young children with bilateral cerebral palsy in Benin: A randomized controlled trial.
Developmental medicine and child neurology·2026
Accelerated long-term forgetting in children with neurofibromatosis type 1.
Developmental medicine and child neurology·2026
Pharmacological and non-pharmacological interventions for managing sleep disorders in children with cerebral palsy: A systematic review.
Developmental medicine and child neurology·2026
Development and validation of the Pediatric Autoimmune encephalitis Severity Scale in children with autoimmune encephalitis.
Developmental medicine and child neurology·2026
Pathophysiology of developmental and/or epileptic encephalopathy with spike-wave activation in sleep: A diagnostic framework.
Developmental medicine and child neurology·2026
Shared dysregulation of complement and phosphorylation pathways in the cerebrospinal fluid of encephalitis, Aicardi-Goutières syndrome, and autism.
Developmental medicine and child neurology·2026
Non-syndromic adult-onset rod-cone dystrophy.
Retina (Philadelphia, Pa.)·2026
Exploring the Landscape of Circular RNAs in Testes of Dezhou Donkey During Distinct Developmental Stages.
Reproduction in domestic animals = Zuchthygiene·2026
Distinguishing different psychiatric disorders using DDx-PRS.
Nature genetics·2026
GFI1 as a novel regulator of γδ T cell development and the IL-17/IFN-γ lineage commitment.
Frontiers in immunology·2026