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Publications by Belinda J McClaren
A Mixed Methods Exploration of Families’ Experiences of the Diagnosis of Childhood Spinal Muscular Atrophy
European Journal of Human Genetics
Genetics
A Mixed Methods Study of Age at Diagnosis and Diagnostic Odyssey for Duchenne Muscular Dystrophy
European Journal of Human Genetics
Genetics
Related publications
Molecular Diagnosis of Spinal and Bulbar Muscular Atrophy in Slovakia
Bratislava Medical Journal
Incidence, Prevalence, and Gene Frequency Studies of Chronic Childhood Spinal Muscular Atrophy.
Journal of Medical Genetics
Genetics
Non-Invasive Prenatal Diagnosis of Spinal Muscular Atrophy by Relative Haplotype Dosage
European Journal of Human Genetics
Genetics
Characteristic of the Spinal Muscular Atrophy Cell Model
Spinal Muscular Atrophy Type 1
Pediatric Critical Care Medicine
Child Health
Critical Care
Pediatrics
Perinatology
Intensive Care Medicine
Spinal Muscular Atrophy Diagnosis and Carrier Screening From Genome Sequencing Data
Genetics in Medicine
Medicine
Genetics
Current and Future Treatments of Spinal Muscular Atrophy
Developmental Medicine and Child Neurology
Child Health
Developmental Neuroscience
Pediatrics
Perinatology
Neurology
Pathogenesis of Proximal Autosomal Recessive Spinal Muscular Atrophy
Acta Neuropathologica
Forensic Medicine
Molecular Neuroscience
Pathology
Neurology
Cellular
Autonomic Dysfunction in Spinal Muscular Atrophy
Turkiye Klinikleri Pediatri
Child Health
Pediatrics
Perinatology