[HTML][HTML] Two additional males with X‐linked, syndromic mental retardation carry de novo mutations in HNRNPH2
WM Jepsen, K Ramsey, S Szelinger, L Llaci… - Clinical …, 2019 - ncbi.nlm.nih.gov
WM Jepsen, K Ramsey, S Szelinger, L Llaci, C Balak, N Belnap, C Bilagody, M De Both…
Clinical genetics, 2019•ncbi.nlm.nih.govTwo additional males with X‐linked, syndromic mental retardation carry de novo mutations in
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HNRNPH2 - PMC Back to Top Skip to main content NIH NLM Logo Access keys NCBI
Homepage MyNCBI Homepage Main Content Main Navigation Search PMC Full-Text Archive
Search in PMC Advanced Search User Guide Journal List Wiley-Blackwell Online Open
PMC6852257 Other Formats PDF (885K) Actions Cite Collections Share Permalink Copy
RESOURCES Similar articles Cited by other articles Links to NCBI Databases Journal List …
Abstract
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