TY - JOUR
T1 - Correction
T2 - A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome (Genetics in Medicine, (2020), 22, 5, (867-877), 10.1038/s41436-019-0743-3)
AU - Genomics England Research Consortium
AU - Cuvertino, Sara
AU - Hartill, Verity
AU - Colyer, Alice
AU - Garner, Terence
AU - Nair, Nisha
AU - Al-Gazali, Lihadh
AU - Canham, Natalie
AU - Faundes, Victor
AU - Flinter, Frances
AU - Hertecant, Jozef
AU - Holder-Espinasse, Muriel
AU - Jackson, Brian
AU - Lynch, Sally Ann
AU - Nadat, Fatima
AU - Narasimhan, Vagheesh M.
AU - Peckham, Michelle
AU - Sellers, Robert
AU - Seri, Marco
AU - Montanari, Francesca
AU - Southgate, Laura
AU - Squeo, Gabriella Maria
AU - Trembath, Richard
AU - van Heel, David
AU - Venuto, Santina
AU - Weisberg, Daniel
AU - Stals, Karen
AU - Ellard, Sian
AU - Barton, Anne
AU - Kimber, Susan J.
AU - Sheridan, Eamonn
AU - Merla, Giuseppe
AU - Stevens, Adam
AU - Johnson, Colin A.
AU - Banka, Siddharth
N1 - Publisher Copyright:
© 2020, The Author(s).
PY - 2020/5/1
Y1 - 2020/5/1
N2 - Correction to: Genetics in Medicine 22:2020 https://doi.org/10.1038/s41436-019-0743-3 published online 17 January 2020. An incorrect reference was cited in the fourth sentence of the Results section. The correct citation should have been Al-Gazali LI, Hamid Z, Hertecant J et al. An autosomal recessive syndrome of choanal atresia, hypothelia/athelia and thyroid gland anomalies overlapping Bamforth syndrome, ANOTHER syndrome and methimazole embryopathy. Clin Dysmorphol 2002;2:79–85. This has now been corrected in both the PDF and HTML versions of the Article.
AB - Correction to: Genetics in Medicine 22:2020 https://doi.org/10.1038/s41436-019-0743-3 published online 17 January 2020. An incorrect reference was cited in the fourth sentence of the Results section. The correct citation should have been Al-Gazali LI, Hamid Z, Hertecant J et al. An autosomal recessive syndrome of choanal atresia, hypothelia/athelia and thyroid gland anomalies overlapping Bamforth syndrome, ANOTHER syndrome and methimazole embryopathy. Clin Dysmorphol 2002;2:79–85. This has now been corrected in both the PDF and HTML versions of the Article.
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U2 - 10.1038/s41436-020-0784-7
DO - 10.1038/s41436-020-0784-7
M3 - Comment/debate
C2 - 32203228
AN - SCOPUS:85082190394
SN - 1098-3600
VL - 22
SP - 980
JO - Genetics in Medicine
JF - Genetics in Medicine
IS - 5
ER -