Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by B. Zabel
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
Wolcott-Rallison Syndrome: Clinical, Genetic, and Functional Study of EIF2AK3 Mutations and Suggestion of Genetic Heterogeneity
Diabetes
Internal Medicine
Endocrinology
Metabolism
Diabetes
Related publications
Prader-Willi, Angelman, and 15q11-Q13 Duplication Syndromes
Pediatric Clinics of North America
Child Health
Pediatrics
Perinatology
Molecular Cytogenetics of Prader-Willi and Angelman Syndromes
The Lancet
Medicine
A Rapid, PCR Based Test for Differential Molecular Diagnosis of Prader-Willi and Angelman Syndromes.
Journal of Medical Genetics
Genetics
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
Establishment of the First WHO International Genetic Reference Panel for Prader Willi and Angelman Syndromes
European Journal of Human Genetics
Genetics
Diagnostic Testing for Prader-Willi Syndrome and Angelman Syndrome: A Cost Comparison
Genetics in Medicine
Medicine
Genetics
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
Linkage Analysis With Chromosome 15q11-13 Markers Shows Genomic Imprinting in Familial Angelman Syndrome.
Journal of Medical Genetics
Genetics
Prader-Willi Syndrome
