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author Sobering, Andrew K.
Bryant, Laura M.
Li, Dong
McGaughran, Julie
Maystadt, Isabelle
Moortgat, Stephanie
Graham, John M.
van Haeringen, Arie
Ruivenkamp, Claudia
Cuperus, Roos
Vogt, Julie
Morton, Jenny
Brasch-Andersen, Charlotte
Steenhof, Maria
Hansen, Lars Kjærsgaard
Adler, Élodie
Lyonnet, Stanislas
Pingault, Veronique
Sandrine, Marlin
Ziegler, Alban
Donald, Tyhiesia
Nelson, Beverly
Holt, Brandon
Petryna, Oleksandra
Firth, Helen
McWalter, Kirsty
Zyskind, Jacob
Telegrafi, Aida
Juusola, Jane
Person, Richard
Bamshad, Michael J.
Earl, Dawn
Chun-Hui Tsai, Anne
Yearwood, Katherine R.
Marco, Elysa
Nowak, Catherine
Douglas, Jessica
Hakonarson, Hakon
Bhoj, Elizabeth J.
author_facet Sobering, Andrew K.
Bryant, Laura M.
Li, Dong
McGaughran, Julie
Maystadt, Isabelle
Moortgat, Stephanie
Graham, John M.
van Haeringen, Arie
Ruivenkamp, Claudia
Cuperus, Roos
Vogt, Julie
Morton, Jenny
Brasch-Andersen, Charlotte
Steenhof, Maria
Hansen, Lars Kjærsgaard
Adler, Élodie
Lyonnet, Stanislas
Pingault, Veronique
Sandrine, Marlin
Ziegler, Alban
Donald, Tyhiesia
Nelson, Beverly
Holt, Brandon
Petryna, Oleksandra
Firth, Helen
McWalter, Kirsty
Zyskind, Jacob
Telegrafi, Aida
Juusola, Jane
Person, Richard
Bamshad, Michael J.
Earl, Dawn
Chun-Hui Tsai, Anne
Yearwood, Katherine R.
Marco, Elysa
Nowak, Catherine
Douglas, Jessica
Hakonarson, Hakon
Bhoj, Elizabeth J.
author_sort Sobering, Andrew K.
collection PubMed
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spelling pubmed-97923862022-12-28 Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology Sobering, Andrew K. Bryant, Laura M. Li, Dong McGaughran, Julie Maystadt, Isabelle Moortgat, Stephanie Graham, John M. van Haeringen, Arie Ruivenkamp, Claudia Cuperus, Roos Vogt, Julie Morton, Jenny Brasch-Andersen, Charlotte Steenhof, Maria Hansen, Lars Kjærsgaard Adler, Élodie Lyonnet, Stanislas Pingault, Veronique Sandrine, Marlin Ziegler, Alban Donald, Tyhiesia Nelson, Beverly Holt, Brandon Petryna, Oleksandra Firth, Helen McWalter, Kirsty Zyskind, Jacob Telegrafi, Aida Juusola, Jane Person, Richard Bamshad, Michael J. Earl, Dawn Chun-Hui Tsai, Anne Yearwood, Katherine R. Marco, Elysa Nowak, Catherine Douglas, Jessica Hakonarson, Hakon Bhoj, Elizabeth J. HGG Adv Correction Elsevier 2022-12-20 /pmc/articles/PMC9792386/ /pubmed/36583168 http://dx.doi.org/10.1016/j.xhgg.2022.100168 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Correction
Sobering, Andrew K.
Bryant, Laura M.
Li, Dong
McGaughran, Julie
Maystadt, Isabelle
Moortgat, Stephanie
Graham, John M.
van Haeringen, Arie
Ruivenkamp, Claudia
Cuperus, Roos
Vogt, Julie
Morton, Jenny
Brasch-Andersen, Charlotte
Steenhof, Maria
Hansen, Lars Kjærsgaard
Adler, Élodie
Lyonnet, Stanislas
Pingault, Veronique
Sandrine, Marlin
Ziegler, Alban
Donald, Tyhiesia
Nelson, Beverly
Holt, Brandon
Petryna, Oleksandra
Firth, Helen
McWalter, Kirsty
Zyskind, Jacob
Telegrafi, Aida
Juusola, Jane
Person, Richard
Bamshad, Michael J.
Earl, Dawn
Chun-Hui Tsai, Anne
Yearwood, Katherine R.
Marco, Elysa
Nowak, Catherine
Douglas, Jessica
Hakonarson, Hakon
Bhoj, Elizabeth J.
Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology
title Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology
title_full Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology
title_fullStr Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology
title_full_unstemmed Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology
title_short Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology
title_sort variants in phf8 cause a spectrum of x-linked neurodevelopmental disorders and facial dysmorphology
topic Correction
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9792386/
https://www.ncbi.nlm.nih.gov/pubmed/36583168
http://dx.doi.org/10.1016/j.xhgg.2022.100168
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