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Publications by E.E. Eichler
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
Human Copy Number Polymorphic Genes
Cytogenetic and Genome Research
Genetics
Molecular Biology
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
