Publication
| Bækgaard CH, Lester EB, Møller-Larsen S, Lauridsen MF, Larsen MJ, NanoImprint: A DNA methylation tool for clinical interpretation and diagnosis of common imprinting disorders using nanopore long-read sequencing Annals of human genetics: 2024 |
| PubMed ID: 38690755 |
|
| Records Return:
(2)
|
|
|
|
|
| Catalog ID | Sex | Age at Sampling | Family | Relationship | Description | Collection_Type_id |
| GM13553 | Male | 17 YR | 2996 | proband | PRADER-WILLI SYNDROME; PWS | GM |
| GM20409 | Male | 6 YR | | proband | ANGELMAN SYNDROME; AS | GM |
|
|
|