Biallelic sequence variants in INTS1 in patients with developmental delays, cataracts, and craniofacial anomalies

M Krall, S Htun, RE Schnur, Alice Brooks, L Baker, AD Campomanes, RE Lamont, KW Gripp, D Schneidman-Duhovny, AM Innes, Grazia Verheijen - Mancini, AM Slavotinek

Research output: Contribution to journalArticleAcademicpeer-review

19 Citations (Scopus)
Original languageUndefined/Unknown
Pages (from-to)582-593
Number of pages12
JournalEuropean Journal of Human Genetics
Issue number4
Publication statusPublished - 2019

Research programs

  • EMC OR-01

Cite this