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Phenotype of a child with Angelman syndrome born to a woman with Prader–Willi syndrome |
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| Authors: | John R. Ostergaard |
| Affiliation: | Department of Pediatrics, Centre for Rare Diseases, Aarhus University Hospital, Aarhus, Denmark |
| Abstract: | |
| Keywords: | Angelman syndrome chromosome 15q11.2‐q13 deletion genetic imprinting Prader– Willi syndrome |