| scholarly article | Q13442814 |
| P50 | author | Baraitser M | Q74872512 |
| P2093 | author name string | Wilson J | |
| Robb SA | |||
| Brett EM | |||
| Pohl KR | |||
| P2860 | cites work | Angelman (happy puppet) syndrome in a girl and her brother | Q33674901 |
| The Angelman ("happy puppet") syndrome | Q34278541 | ||
| The puppet-like syndrome of Angelman | Q34282653 | ||
| The "happy puppet" syndrome | Q36061447 | ||
| The “Happy Puppet” Syndrome: Two New Cases and a Review of Five Previous Cases | Q39959849 | ||
| Three more 'Happy Puppets' | Q41938009 | ||
| Angelman's ("Happy Puppet") Syndrome | Q41938322 | ||
| The Angelman (Happy Puppet) syndrome: is it autosomal recessive? | Q51199570 | ||
| The Angelman syndrome in two brothers. | Q51246659 | ||
| Behavioral correlates in the happy puppet syndrome: a characteristic profile? | Q51252688 | ||
| The "happy puppet" syndrome in two siblings. | Q51270656 | ||
| Fourteen Happy Puppets | Q51297410 | ||
| Abstracts of the meeting of the Clinical Genetics Society. 20 and 21 November 1987, London. (Joint meeting with the Skeletal Dysplasia Group) | Q68350355 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 83-86 | |
| P577 | publication date | 1989-01-01 | |
| P1433 | published in | Archives of Disease in Childhood | Q4787296 |
| P1476 | title | The 'happy puppet' syndrome of Angelman: review of the clinical features | |
| P478 | volume | 64 |
| Q41640527 | Angelman syndrome |
| Q24681713 | Angelman syndrome resulting from UBE3A mutations in 14 patients from eight families: clinical manifestations and genetic counselling |
| Q30252074 | Angelman syndrome: A review highlighting musculoskeletal and anatomical aberrations |
| Q36340020 | Angelman syndrome: clinical profile |
| Q68038171 | Angelman's syndrome |
| Q52195427 | Angelman's syndrome: clinical and electroencephalographic findings. |
| Q37284693 | Behavior and neuropsychiatric manifestations in Angelman syndrome. |
| Q40548520 | Behaviour problems in Angelman syndrome |
| Q33683182 | Clinical features in 27 patients with Angelman syndrome resulting from DNA deletion. |
| Q48317479 | Clinical research on Angelman syndrome in the United Kingdom: Observations on 82 affected individuals |
| Q41075704 | Communication development in Angelman's syndrome |
| Q48158829 | Diagnosis of Angelman syndrome: clinical and EEG criteria |
| Q37732476 | Epilepsy in patients with Angelman syndrome |
| Q28593439 | Genetic ablation of the steroid receptor coactivator-ubiquitin ligase, E6-AP, results in tissue-selective steroid hormone resistance and defects in reproduction |
| Q100428064 | Imitation in Angelman syndrome: the role of social engagement |
| Q72209589 | Molecular study of chromosome 15 in 22 patients with Angelman syndrome |
| Q48354837 | Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation. |
| Q33912426 | Mutations affecting GABAergic signaling in seizures and epilepsy |
| Q34462834 | Novel deletion of the E3A ubiquitin protein ligase gene detected by multiplex ligation-dependent probe amplification in a patient with Angelman syndrome |
| Q41924626 | Paternal UPD15: further genetic and clinical studies in four Angelman syndrome patients |
| Q38781012 | Quantitative Measurement of Communication Ability in Children with Angelman Syndrome |
| Q37966441 | Rett syndrome and the autistic disorders. |
| Q37090067 | The Drosophila homologue of the Angelman syndrome ubiquitin ligase regulates the formation of terminal dendritic branches |
| Q35143079 | Ube3a imprinting impairs circadian robustness in Angelman syndrome models |
| Q73427845 | Unexpected familial recurrence in Angelman syndrome |
| Q52194097 | [Angelman syndrome: a frequently undiagnosed cause of mental retardation and epilepsy. Case report] |
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