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Two additional males with X‐linked, syndromic mental retardation carry de novo mutations in HNRNPH2
[Image: see text]
| Autores principales: | , , , , , , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Blackwell Publishing Ltd
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852257/ https://www.ncbi.nlm.nih.gov/pubmed/31236915 http://dx.doi.org/10.1111/cge.13580 |
| _version_ | 1783469790655938560 |
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| author | 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. |
| author_facet | 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. |
| author_sort | Jepsen, Wayne M. |
| collection | PubMed |
| description | [Image: see text] |
| format | Online Article Text |
| id | pubmed-6852257 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2019 |
| publisher | Blackwell Publishing Ltd |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-68522572019-11-22 Two additional males with X‐linked, syndromic mental retardation carry de novo mutations in HNRNPH2 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. Clin Genet Letter to the Editor [Image: see text] Blackwell Publishing Ltd 2019-06-24 2019-08 /pmc/articles/PMC6852257/ /pubmed/31236915 http://dx.doi.org/10.1111/cge.13580 Text en © 2019 The Authors Clinical Genetics Published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
| spellingShingle | Letter to the Editor 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. Two additional males with X‐linked, syndromic mental retardation carry de novo mutations in HNRNPH2 |
| title | Two additional males with X‐linked, syndromic mental retardation carry de novo mutations in HNRNPH2
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| title_full | Two additional males with X‐linked, syndromic mental retardation carry de novo mutations in HNRNPH2
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| title_fullStr | Two additional males with X‐linked, syndromic mental retardation carry de novo mutations in HNRNPH2
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| title_full_unstemmed | Two additional males with X‐linked, syndromic mental retardation carry de novo mutations in HNRNPH2
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| title_short | Two additional males with X‐linked, syndromic mental retardation carry de novo mutations in HNRNPH2
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| title_sort | two additional males with x‐linked, syndromic mental retardation carry de novo mutations in hnrnph2 |
| topic | Letter to the Editor |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852257/ https://www.ncbi.nlm.nih.gov/pubmed/31236915 http://dx.doi.org/10.1111/cge.13580 |
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