Abstract
(The American Journal of Human Genetics 106, 356–370; March 5, 2020) In the version of this paper originally published, the underlying cause for Hunter McAlpine syndrome was incorrectly described in Table 1. The relevant description has been changed to read “Chr5q35-qter duplication involving NSD1” in the updated Table 1 reflected here. The authors apologize for this error.
Original language | English |
---|---|
Pages (from-to) | 1161-1163 |
Number of pages | 3 |
Journal | American Journal of Human Genetics |
Volume | 108 |
Issue number | 6 |
DOIs |
|
Publication status | Published or Issued - 3 Jun 2021 |
ASJC Scopus subject areas
- Genetics
- Genetics(clinical)
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}
In: American Journal of Human Genetics, Vol. 108, No. 6, 03.06.2021, p. 1161-1163.
Research output: Contribution to journal › Comment/debate › peer-review
TY - JOUR
T1 - Erratum
T2 - Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders (The American Journal of Human Genetics (2020) 106(3) (356–370), (S0002929720300197), (10.1016/j.ajhg.2020.01.019))
AU - Aref-Eshghi, Erfan
AU - Kerkhof, Jennifer
AU - Pedro, Victor P.
AU - France, Groupe DI
AU - Barat-Houari, Mouna
AU - Ruiz-Pallares, Nathalie
AU - Andrau, Jean Christophe
AU - Lacombe, Didier
AU - Van-Gils, Julien
AU - Fergelot, Patricia
AU - Dubourg, Christéle
AU - Cormier-Daire, Valerie
AU - Rondeau, Sophie
AU - Lecoquierre, François
AU - Saugier-Veber, Pascale
AU - Nicolas, Gaël
AU - Lesca, Gaetan
AU - Chatron, Nicolas
AU - Sanlaville, Damien
AU - Vitobello, Antonio
AU - Faivre, Laurence
AU - Thauvin-Robinet, Christel
AU - Laumonnier, Frederic
AU - Raynaud, Martine
AU - Alders, Mariëlle
AU - Mannens, Marcel
AU - Henneman, Peter
AU - Hennekam, Raoul C.
AU - Velasco, Guillaume
AU - Francastel, Claire
AU - Ulveling, Damien
AU - Ciolfi, Andrea
AU - Pizzi, Simone
AU - Tartaglia, Marco
AU - Heide, Solveig
AU - Héron, Delphine
AU - Mignot, Cyril
AU - Keren, Boris
AU - Whalen, Sandra
AU - Afenjar, Alexandra
AU - Bienvenu, Thierry
AU - Campeau, Philippe M.
AU - Rousseau, Justine
AU - Levy, Michael A.
AU - Brick, Lauren
AU - Kozenko, Mariya
AU - Balci, Tugce B.
AU - Siu, Victoria Mok
AU - Stuart, Alan
AU - Kadour, Mike
AU - Masters, Jennifer
AU - Takano, Kyoko
AU - Kleefstra, Tjitske
AU - de Leeuw, Nicole
AU - Field, Michael
AU - Shaw, Marie
AU - Gecz, Jozef
AU - Ainsworth, Peter J.
AU - Lin, Hanxin
AU - Rodenhiser, David I.
AU - Friez, Michael J.
AU - Tedder, Matt
AU - Lee, Jennifer A.
AU - DuPont, Barbara R.
AU - Stevenson, Roger E.
AU - Skinner, Steven A.
AU - Schwartz, Charles E.
AU - Genevieve, David
AU - Sadikovic, Bekim
N1 - Publisher Copyright: © 2021 American Society of Human Genetics
PY - 2021/6/3
Y1 - 2021/6/3
N2 - (The American Journal of Human Genetics 106, 356–370; March 5, 2020) In the version of this paper originally published, the underlying cause for Hunter McAlpine syndrome was incorrectly described in Table 1. The relevant description has been changed to read “Chr5q35-qter duplication involving NSD1” in the updated Table 1 reflected here. The authors apologize for this error.
AB - (The American Journal of Human Genetics 106, 356–370; March 5, 2020) In the version of this paper originally published, the underlying cause for Hunter McAlpine syndrome was incorrectly described in Table 1. The relevant description has been changed to read “Chr5q35-qter duplication involving NSD1” in the updated Table 1 reflected here. The authors apologize for this error.
UR - http://www.scopus.com/inward/record.url?scp=85107089857&partnerID=8YFLogxK
U2 - 10.1016/j.ajhg.2021.04.022
DO - 10.1016/j.ajhg.2021.04.022
M3 - Comment/debate
C2 - 34087165
AN - SCOPUS:85107089857
SN - 0002-9297
VL - 108
SP - 1161
EP - 1163
JO - American Journal of Human Genetics
JF - American Journal of Human Genetics
IS - 6
ER -