Two additional males with X‐linked, syndromic mental retardation carry de novo mutations in HNRNPH2. Issue 2 (24th June 2019)

• Record Type: Journal Article
• Authors: Jepsen, Wayne M.; Ramsey, Keri; Szelinger, Szabolcs; Llaci, Lorida; Balak, Chris; Belnap, Newell; Bilagody, Cherae; De Both, Matthew; Gupta, Raj; Naymik, Marcus; Pandey, Richa; Piras, Ignazio S.; Sanchez‐Castillo, Meredith; Rangasamy, Sampathkumar; Narayanan, Vinodh; Huentelman, Matthew J.
• Is Part Of: Clinical genetics. Volume 96:Issue 2(2019)
• Page Start: 183
• Page End: 185
• Publication Date: 2019-06-24
• Subjects: Medical genetics -- Periodicals; 616.0420
• DOI: 10.1111/cge.13580
• Languages: English
• ISSNs: 0009-9163

Abstract

Abstract :