Genome sequencing identifies KMT2E ‐disrupting cryptic structural variant in a female with O'Donnell‐Luria‐Rodan syndrome

Hashim M., Stewart H., Yu J., Banos‐Pinero B., Pagnamenta AT., Taylor JC.

DOI

10.1111/cge.14355

Type

Journal article

Publisher

Wiley

Publication Date

2023-09-01T00:00:00+00:00

Volume

104

Pages

390 - 392

Total pages

2

Permalink More information Close