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Author/Creator Pandey, Richa

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

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.
Journal:
Clinical genetics
Issue:
Volume 96:Issue 2(2019)
Page Start:
183
Record Type:
Journal Article
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