Publication
| Knoll JH, Nicholls RD, Magenis RE, Graham JM Jr, Lalande M, Latt SA, Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion. Am J Med Genet32:285-90 1989 |
| PubMed ID: 2564739 |
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| Records Return:
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| Catalog ID | Gender | Age at Sampling | Family | Relationship | Description | Collection_Type_id |
| GM11516 | Female | 4 YR | 1396 | proband | ANGELMAN SYNDROME; AS | GM |
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