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Publications by J.H.M. Knoll
Identification of Four Highly Conserved Genes Between Breakpoint Hotspots BP1 and BP2 of the Prader-Willi/Angelman Syndromes Deletion Region That Have Undergone Evolutionary Transposition Mediated by Flanking Duplicons
American Journal of Human Genetics
Genetics
Related publications
Molecular Cytogenetics of Prader-Willi and Angelman Syndromes
The Lancet
Medicine
Prader-Willi, Angelman, and 15q11-Q13 Duplication Syndromes
Pediatric Clinics of North America
Child Health
Pediatrics
Perinatology
Exploring Autism Symptoms in an Australian Cohort of Patients With Prader-Willi and Angelman Syndromes
Journal of Neurodevelopmental Disorders
Pediatrics
Cognitive Neuroscience
Perinatology
Neurology
Forensic Medicine
Child Health
Pathology
A Rapid, PCR Based Test for Differential Molecular Diagnosis of Prader-Willi and Angelman Syndromes.
Journal of Medical Genetics
Genetics
Establishment of the First WHO International Genetic Reference Panel for Prader Willi and Angelman Syndromes
European Journal of Human Genetics
Genetics
A Putative Gene Family in 15q11-13 and 16p11.2: Possible Implications for Prader-Willi and Angelman Syndromes.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
PCR-based Molecular Diagnosis of Prader-Willi and Angelman Syndromes Using Restriction Analysis After Bisulfite Treatment. Potential for Quantitative Estimation
Genetics in Medicine
Medicine
Genetics
Diagnostic Testing for Prader-Willi Syndrome and Angelman Syndrome: A Cost Comparison
Genetics in Medicine
Medicine
Genetics
Anaesthetic Considerations in the Prader-Willi Syndrome: Report of Four Cases
Canadian Journal of Anaesthesia
Medicine
Anesthesiology
Pain Medicine
