Iqbal, Maria http://orcid.org/0000-0003-2777-0198
Maroofian, Reza
Çavdarlı, Büşranur
Riccardi, Florence
Field, Michael
Banka, Siddharth
Bubshait, Dalal K.
Li, Yun
Hertecant, Jozef
Baig, Shahid Mahmood
Dyment, David
Efthymiou, Stephanie
Abdullah, Uzma
Makhdoom, Ehtisham Ul Haq
Ali, Zafar
Scherf de Almeida, Tobias
Molinari, Florence
Mignon-Ravix, Cécile
Chabrol, Brigitte
Antony, Jayne
Ades, Lesley
Pagnamenta, Alistair T.
Jackson, Adam
Douzgou, Sofia
Ambrose, J.C.
Arumugam, P.
Bleda, M.
Boardman-Pretty, F.
Boustred, C.R.
Brittain, H.
Caulfield, M.J.
Chan, G.C.
Fowler, T.
Giess, A.
Hamblin, A.
Henderson, S.
Hubbard, T.J.P.
Jackson, R.
Jones, L.J.
Kasperaviciute, D.
Kayikci, M.
Kousathanas, A.
Lahnstein, L.
Leigh, S.E.A.
Leong, I.U.
Lopez, F.J.
Maleady-Crowe, F.
Moutsianas, L.
Mueller, M.
Murugaesu, N.
Need, A.C.
O’Donovan, P.
Odhams, C.A.
Patch, C.
Perez-Gil, D.
Pereira, M.B.
Pullinger, J.
Rahim, T.
Rendon, A.
Rogers, T.
Savage, K.
Sawant, K.
Scott, R.H.
Siddiq, A.
Sieghart, A.
Smith, S.C.
Sosinsky, A.
Stuckey, A.
Tanguy, M.
Thomas, E.R.A.
Thompson, S.R.
Tucci, A.
Walsh, E.
Welland, M.J.
Williams, E.
Witkowska, K.
Wood, S.M.
Beetz, Christian
Karageorgou, Vasiliki
Vona, Barbara
Rad, Aboulfazl
Baig, Jamshaid Mahmood
Sultan, Tipu
Alvi, Javeria Raza
Maqbool, Shazia
Rahman, Fatima
Toosi, Mehran Beiraghi
Ashrafzadeh, Farah
Imannezhad, Shima
Karimiani, Ehsan Ghayoor
Sarwar, Yasra
Khan, Sheraz
Jameel, Muhammad
Noegel, Angelika A.
Budde, Birgit
Altmüller, Janine
Motameny, Susanne
Höhne, Wolfgang
Houlden, Henry
Nürnberg, Peter
Wollnik, Bernd
Villard, Laurent
Alkuraya, Fowzan Sami
Osmond, Matthew
Hussain, Muhammad Sajid
Yigit, Gökhan
Funding for this research was provided by:
Higher Education Commission, Pakistan
Center for Molecular Medicine Cologne, University of Cologne (2635/8029/01)
Köln Fortune Program, Faculty of Medicine, University of Cologne (381/2020)
Deutsche Forschungsgemeinschaft (EXC 2067/1- 390729940)
Medical Research Council (MR/S01165X/1, MR/S005021/1, G0601943)
This article is maintained by: Elsevier
Article Title: Biallelic variants in PCDHGC4 cause a novel neurodevelopmental syndrome with progressive microcephaly, seizures, and joint anomalies
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-021-01260-4
Content Type: article
Copyright: © 2021, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics